US5329010A - Quinone derivatives - Google Patents

Quinone derivatives Download PDF

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US5329010A
US5329010A US07/840,862 US84086292A US5329010A US 5329010 A US5329010 A US 5329010A US 84086292 A US84086292 A US 84086292A US 5329010 A US5329010 A US 5329010A
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pharmacologically acceptable
acceptable salt
quinone derivative
lower alkoxy
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Yasushi Okamoto
Katsuya Tagami
Shigeki Hibi
Hirotoshi Numata
Tetsuya Kawahara
Naoki Kobayashi
Masanobu Shinoda
Koukichi Harada
Kaname Miyamoto
Koichi Abe
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Eisai R&D Management Co Ltd
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Eisai Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/56—Amides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/55—Acids; Esters

Definitions

  • the present invention relates to a quinone derivative exhibiting an excellent activity as a drug.
  • leukotrienes and thromboxanes have recently been noticed. They each cause inflammation alone or interact with each other to cause it, or participate in the continuation of inflammation.
  • few compounds exhibiting both leukotrienes production-inhibiting activity and thromboxanes production-inhibiting activity have been found.
  • the inventors of the present invention have made intensive studies for many years to obtain a compound exhibiting both of the above-mentioned activities and have found that a quinone derivative which will be described below exhibits both the activities at a well-balanced activity ratio and is excellent as a so-called dual inhibitor.
  • the present invention has been accomplished on the basis of this finding.
  • the present invention provides a quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR3## wherein A stands for a group represented by the formula: ##STR4## (wherein R 3 , R 4 and R 5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R 3 and R 4 are not simultaneously each a lower alkoxy group) or a group represented by the formula: ##STR5## (wherein R 3 , R 4 and R 5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group
  • quinone derivatives or pharmacologically acceptable salts thereof of the present invention include derivatives where R 1 in the general formula (I) is a heteroarylalkyl group, where R 3 in the genaral formula (I) is a lower alkoxy group, where R 4 in the general formula (I) is a lower alkyl group, where R 5 in the general formula (I) is a lower alkyl group, where X in the general formula (I) is a hydroxy group or a alkoxy group, where Y in the general formula (I) is a hydroxy group or a alkoxy group and where B in the general formula (I) is a carboxyl group.
  • quinone derivatives or pharmacologically acceptable salts thereof of the present invention include derivatives where R 1 in the general formula (I) is a pyridylhexyl group or a pyridylpentyl group, where R 3 in the general formula (I) is a methoxy group or a methyl group, where R 4 in the general formula (I) is a methyl group or a methoxy group, where R 5 in the general formula (I) is a methyl group or a methoxy group, where X in the general formula (I) is a hydroxy group or a methoxy group and where Y in the general formula (I) is a hydroxy group or a methoxy group.
  • the quinone derivative portion of the quinone derivative or pharmacologically acceptable salt thereof of the present invention is still advantageously (E)-3-(2-methoxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid.
  • the present invention also provides leukotrienes production inhibitor and/or thromboxanes production inhibitor comprising a quinone derivative or pharmacologically acceptable salt thereof of the present invention as an active ingredient.
  • the present invention further provides a therapeutic and preventive agent for diseases for which leukotrienes production inhibitor and/or thromboxanes inhibitor are efficacious, which comprise a quinone derivative or pharmacologically acceptable salt thereof of the present invention as an active ingredient.
  • the present invention provides a pharmacological composition which comprises a therapeutically effective amount of the quinone derivative or a pharmacologically acceptable salt thereof of the present invention and a pharmacologically acceptable vehicle.
  • the present invention also provides use of a quinone derivative or a pharmacologically acceptable salt thereof of the present invention for the making of a medicament for treating a disease in which the production of leukotriene is elevated, and/or, a disease in which the production of thromboxane A 2 is elevated.
  • the present invention further provides use of a quinone derivative or a pharmacologically acceptable salt thereof of the present invention for the making of a medicament for treating a disease selected from the group consisting of asthma, chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus, cirrhosis, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency, nephrosis and nephritis.
  • a disease selected from the group consisting of asthma, chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus, cirrhosis, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency, nephrosis and neph
  • the present invention provides a method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof of the present invention to a patient suffering from a disease in which the production of leukotriene is elevated, and/or, a patient suffering from a disease in which the production of thromboxane A 2 is elevated.
  • the present invention also provides a method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof of the present invention to a patient suffering from a disease selected from the group consisting of asthma, chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus, cirrhosis, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency, nephrosis and nephritis.
  • a disease selected from the group consisting of asthma, chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus, cirrhosis, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency,
  • the compound of the present invention is a quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR6## wherein A stands for a group represented by the formula: ##STR7## (wherein R 3 , R 4 and R 5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R 3 and R 4 are not simultaneously each a lower alkoxy group) or a group represented by the formula: ##STR8## (wherein R 3 , R 4 and R 5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyal
  • R 1 stands for a heteroarylalkyl group
  • B stands for a carboyxl group or a protected carboxyl group.
  • the lower alkyl group defined with respect to R 3 , R 4 and R 5 is a straight-chain or branched alkyl group having 1 to 8 carbon atoms and examples thereof include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, n-pentyl(amyl) group, isopentyl group, neopentyl group, tert-pentyl group, 1-methylbutyl group, 2-methylbutyl group, 3-methylbutyl, 1,2-dimethylpropyl group, n-hexyl group, isohexyl group, 1-methylpentyl group, 2-methylpentyl group, 3-methylpentyl group, 1,1-dimethylbutyl group, 1,2-dimethylbutyl group, 2,2-dimethyl
  • the lower alkoxy group defined with respect to R 3 , R 4 and R 5 is one derived from the above-mentioned lower alkyl group and examples thereof include methoxy group, ethoxy group and n-propoxy group, among which a methoxy group is most desirable.
  • the alkoxy group constituting the alkoxyalkyl group defined with respect to R 3 , R 4 and R 5 has 1 to 8 carbon atoms, preferably 1 to 2 carbon atoms, while the alkyl group, i.e., the alkylene chain constituting it has 1 to 10 carbon atoms.
  • the alkoxyalkoxy group defined with respect to R 3 R 4 and R 5 is one derived from the above-mentioned lower alkoxy group and examples thereof include methoxymethoxy group, methoxyethoxy group, ethoxyethoxy group and methoxypropoxy group.
  • the cycloalkyl group constituting the cycloalkylalkoxy group defined with respect to R 3 , R 4 and R 5 has 3 to 7 carbon atoms, preferably 5 or 6 carbon atoms, while the alkoxy group constituting it is as defined above with respect to the lower alkoxy group.
  • the alkyl group constituting the thioalkyl group defined with respect to R 3 , R 4 and R 5 has 1 to 8 carbon atoms, preferably 1 or 2 carbon atoms.
  • both R 3 and R 4 cannot be each a lower alkoxy group such as a methoxy group simultaneously.
  • R 3 , R 4 and R 5 are a case wherein one of R 3 , R 4 and R 5 is a lower alkoxy group such as a methoxy group and the others are each a lower alkyl group such as a methyl group and ethyl group, which may be the same or different from each other.
  • the heteroaryl group constituting the heteroarylalkyl group defined with respect to R 1 is preferably a 5- or 6-membered nitrogenous heteroaryl group and particular examples thereof include pyridyl group and imidazolyl group, which may be either unsubstituted or each substituted with a lower alkyl group such as a methyl group and ethyl group, a lower alkoxy group such as a methoxy grooup and ethoxy group or a halogen atom such as chlorine atom and bromine atom.
  • the alkyl group constituting the heteroarylalkyl group i.e. the alkylene chain has 1 to 10 carbon atoms, preferably 2 to 8 carbon atoms, still preferably 4 to 6 carbon atoms. Further, the alkylene chain may have a substituted lower alkyl group such as a methyl group and ethyl group at any carbon atom.
  • the protected hydroxyl group defined with respect to X and Y may be, for example, a hydroxyl group protected with the above-mentioned lower alkyl group such as a methyl group and ethyl group, i.e., an alkoxy group, or a hydroxyl group protected with an acyl group such as an acetyl group, propionyl group, butyroyl group, pivaloyl group and nicotinoyl group, i.e., a group having an ester bond.
  • it may be any one which can be deprotected by some means in vivo to regenerate a hydroxyl group.
  • the protective group constituting the protected carboxyl group defined with respect to B includes lower alkyl groups such as methyl group, ethyl group and t-butyl group; lower alkyl groups substituted with a phenyl group which may be substituted, such as p-methoxybenzyl group, p-nitrobenzyl group, 3,4-dimethoxybenzyl group, diphenylmethyl group, trityl (triphenylmethyl) group and phenethyl group; halogenated lower alkyl groups such as 2,2,2-trichloroethyl group and 2-iodoethyl group; lower alkanoyloxy lower alkyl groups such as pivaloyloxymethyl group, acetoxymethyl group, propionyloxymethyl group, butyryloxymethyl group, valeryloxymethyl group, 1-acetoxyethyl group, 2-acetoxyethyl group, 1-pivaloyloxyethyl group and 2-pivaloy
  • the protected carboxyl group may be an acid amide.
  • the protected carboxyl group may be any one which can be deprotected by some means in vivo to regenerate a carboxyl group.
  • the pharmacologically acceptable salt according to the present invention includes inorganic acid salts such as hydrochloride, hydrobromide, sulfate and phosphate; organic acid salts such as acetate, maleate, tartrate, methanesulfonate, benzenesulfonate and toluenesulfonate; and amino acid salts such as argininate, aspartate and glutamate.
  • inorganic acid salts such as hydrochloride, hydrobromide, sulfate and phosphate
  • organic acid salts such as acetate, maleate, tartrate, methanesulfonate, benzenesulfonate and toluenesulfonate
  • amino acid salts such as argininate, aspartate and glutamate.
  • the quinone derivative of the present invention can form a metal salt such as sodium salt, potassium salt, calcium salt and magnesium salt.
  • a metal salt such as sodium salt, potassium salt, calcium salt and magnesium salt.
  • the pharmacologically acceptable salt of the present invention includes these metal salts.
  • the compound of the present invention may be present as geometrical isomers (including cis-and trans-isomers) because it has a double bond in its molecule, it is needless to say that the present invention includes all of the isomers.
  • PREPARATION PROCESS 1 ##STR9## (in the above formulas (II) and (III), X, Y, R 1 , R 3 , R 4 , R 5 and B are each as defined above).
  • the compounds (II) and (III) are compounds of the present invention.
  • the benzoquinone derivative represented by the formula (III) can be prepared by reacting the hydroquinone derivative represented by the formula (II) with an oxidizing agent, while the hydroquinone derivative (II) can be prepared by the reduction of the benzoquinone derivative (III).
  • cerium (IV) ammonium nitrate, ferric chloride hexahydrate or lead oxide is used as an oxidizing agent.
  • the amount of the oxidizing agent to be used is preferably 2 to 10 times by mole as much as the hydroquinone.
  • the preferable solvent to be used in the oxidation includes acetonitrile, benzene, ethyl acetate, dioxane, ethanol, 1,2-dimethoxyethane and mixtures thereof with water.
  • the oxidation is conducted at a reaction temperature of 0° to 80° C., preferably 0° to 20° C.
  • the reaction time is generally about 1 to 12 hours.
  • sodium borohydride or sodium hydrosulfite is preferably used as a reducing agent.
  • the preferable solvent to be used in the reduction includes ethanol, tetrahydrofuran, ethyl acetate, 1,2-dimethoxyethane and mixtures thereof with water.
  • the reaction temperature is preferably 0° to 40° C., still preferably 0° to 20° C.
  • hydroquinone derivative (II') which is one of the objective compounds according to the present invention can be prepared also by the following process: ##STR10## (in the above reaction scheme, R 1 , R 3 , R 4 , R 5 , X and Y are each as defined above;
  • B' is a group selected from among those defined with respect to B except for a carboxyl group).
  • an objective compound represented by the general formula (II') can be prepared by reacting an aldehyde derivative represented by the general formula (IV) with a phosphonate represented by the general formula (V) in the presence of a base through the Wittig reaction [see, e.g., J.A.C.S., 83, 1733(1961)].
  • the base to be used in this reaction includes alkali metal hydrides such as sodium hydride and potassium hydride; and alkali metal alcoholates such as sodium methylate, sodium ethylate and potassium tert-butoxide.
  • alkali metal hydrides such as sodium hydride and potassium hydride
  • alkali metal alcoholates such as sodium methylate, sodium ethylate and potassium tert-butoxide.
  • Preferred examples of the solvent to be used therein include benzene, toluene, dichloromethane, tetrahydrofuran, dioxane, dimethoxyethane and dimethylformamide.
  • the reaction temperature is 0° to 100° C., preferably 20° to 80° C.
  • a hydroquinone derivative represented by the general formula (I) wherein B is a carboxyl group can be prepared by the following process: ##STR11## (in the above reaction scheme, R 1 , R 3 , R 4 , R 5 , X, Y and B' are each as defined above).
  • a compound represented by the general formula (VI) which is one of the objective compounds can be prepared by saponifying a compound represented by the general formula (II') with an alkali according to the conventional process.
  • This saponification is conducted by the use of the conventional alkali such as alcoholic caustic soda or potash.
  • a compound represented by the general formula (I) wherein B is a protected carboxyl group can be prepared by the following process: ##STR13## (in the above reaction scheme, R 1 , R 3 , R 4 , R 5 and B' are each as defined above).
  • the objective compound (II') or (VIII) is an ester, it can be prepared by esterifying a carboxylic acid represented by the general formula (VII) by the conventional process.
  • the solvent to be used in this esterification may be any one which is inert to the esterification.
  • the reaction temperature is not particularly limited, but varies depending upon the kind of the reactive derivative.
  • the objective compound (II') or (VIII) is an amide
  • it can be prepared by converting a carboxylic acid represented by the general formula (VII) or a reactive derivative thereof into a corresponding amide by the conventional process.
  • the reactive derivative of the compound (VII) includes acid halides such as acid chloride and acid bromide; acid azide; active esters thereof with N-hydroxybenzotriazole or N-hydroxysuccinimide; symmetric anhydride; and mixed acid anhydride thereof with alkylcarbonic acid or p-toluenesulfonic acid.
  • the compound (VII) is a free carboxylic acid
  • the amidation is conducted in an organic solvent inert to the amidation, for example, pyridine, tetrahydrofuran, dioxane, ether, benzene, toluene, xylene, methylene chloride, dichloroethane, chloroform, dimethylformamide, ethyl acetate or acetonitrile.
  • organic solvent inert for example, pyridine, tetrahydrofuran, dioxane, ether, benzene, toluene, xylene, methylene chloride, dichloroethane, chloroform, dimethylformamide, ethyl acetate or acetonitrile.
  • the reaction temperature is not particularly limited but varies depending upon the kind of the reactive derivative.
  • Calcium ionophore A-23187 [Calbiochem (registered trademark)] was added in a final concentration of 2 ⁇ g/ml. After the reaction at 37° C. for additional 10 minutes, the plate was put on ice and a BW755C solution was added in a final concentration of 100 ⁇ M. The resulting plate was centrifuged at 15000 rpm for 10 minutes. The supernatant was recovered and the amounts of LTB 4 and TxB 2 in the supernatant were determined by enzyme immunoassay with an EIA kit mfd. by Cayman.
  • Thromboxane A 2 is very unstable to treat and naturally turns to thromboxane B 2 in 10-20 seconds in the human body. Therefore, thromboxane B 2 was used in the tests above).
  • the quinone derivatives according to the present invention are efficacious for diseases for which a leukotriene production-inhibiting activity and/or a thromboxane A 2 production-inhibiting activity is efficacious.
  • diseases include asthma, various liver troubles (such as chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus and cirrhosis), ischemic heart diseases (such as myocardial infarction and angina pectoris), cerebral ischemic diseases (such as cerebral embolism and cerebral thrombosis) and various kidney diseases (such as renal insufficiency, nephrosis and nephritis).
  • various liver troubles such as chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus and cirrhosis
  • ischemic heart diseases such as myo
  • the compounds of the present invention are highly safe and therefore are valuable in this respect.
  • the compounds of the present invention may be each administered orally as a powder, granule, capsule or syrup, or parenterally as a suppository, injections, external preparation or drop.
  • the dose of the compound remarkably varies depending upon the symptom, the age of a patient and the kind of disease, it is generally about 0.1 to 2,000 mg, preferably about 2 to 500 mg, still preferably about 5 to 150 mg per adult a day, which may be administered in one to several portions a day.
  • the compounds of the present invention can be converted into pharmaceutical preparations by the use of the conventional excipients carriers according to the conventional processes.
  • a solid preparation for oral administration according to the present invention is prepared by adding a vehicle and, if necessary, a binder, disintegrator, lubricant, colorant and/or corrigent to an active ingredient and shaping the obtained mixture into a tablet, coated tablet, granule, powder or capsule.
  • Examples of the vehicle include lactose, corn starch, sucrose, glucose, sorbitol, crystalline cellulose and silicon dioxide; those of the binder include polyvinyl alcohol, polyvinyl ether, ethylcellulose, methylcellulose, gum arabic, tragacanth, gelatin, shellac, hydroxypropylcellulose, hydroxylpropylmethylcellulose, calcium citrate, dextrin and pectin; those of the lubricant include magnesium stearate, talc, polyethylene glycol, silica and hardened vegetable oil; those of the colorant include those authorized as pharmaceutical additives; and those of the corrigent include cocoa powder, menthae herba (menthol), aromatic powder, mentha oil (peppermint oil), borneol and powdered cinnamon bark.
  • the tablet and granule may be suitably coated with sugar, gelatin and the like, if necessary.
  • An injection according to the present invention is prepared by adding a pH modifier, buffer, stabilizer and/or solubilizing agent to an active ingredient at need and converting the mixture into an injection for subcutaneous, intramuscular or intravenous administration.
  • n-Bu n-butyl group
  • n-Hep n-heptyl group
  • MOMO methoxymethoxy group
  • sodium hydride (55% oil suspension, 59 g) was suspended in N,N-dimethylformamide (500 ml), followed by the dropwise addition of 300 g of triethyl phosphonoacetate.
  • the obtained mixture was stirred at 50° to 60° C. for one hour, followed by the addition of a solution of the above residue (a pale-red oil) in N,N-dimethylformamide (500 ml).
  • the obtained mixture was stirred at 50° to 60° C. for 18 hours.
  • ethyl acetate (3 l) was added to the reaction mixture and the mixture was washed with a saturated aqueous solution of sodium chloride twice.
  • reaction mixture was poured onto 1 l of ice-water.
  • the obtained mixture was extracted with 1 l of ethyl acetate twice.
  • the organic layer was dried over magnesium sulfate and distilled to remove the solvent.
  • the residue was subjected to silica gel column chromatography [solvent: n-hexane ⁇ ethyl acetate (10% ⁇ 30%)/n-hexane].
  • a hydrochloride of the compound described above (1) was prepared by the conventional process.
  • the obtained mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate twice and thereafter with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and filtered.
  • the filtrate was concentrated to 10 ml, adsorbed on a silica gel column and eluted with an ethyl acetate/n-hexane (1:1) mixture.
  • the fractions containing the objective compound were combined and dry hydrogen chloride gas was bubbled thereinto for one minute.
  • the solvent was distilled away in a vacuum. 0.40 g of the title compound was obtained as a yellow oil.
  • the obtained mixture was stirred at room temperature day and night, followed by the addition of water.
  • the obtained mixture was extracted with ethyl acetate.
  • the organic layer was stirred while bubbling air thereinto for 2 hours, washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated in a vacuum.
  • the residue was purified by silica gel column chromatography (ethyl acetate) to give 0.71 g of the title compound as an orange oil.
  • Example 3 30 and 100 mg/kg of the compound obtained in the Example 3 was orally administered to female Slc:SD rats aged 7 weeks (each group consisting of 5 animals) for 4 weeks. This compound was suspended in a 0.5 wt. % aqueous solution of methylcellulose and administered once a day.
  • Example 3 30 and 100 mg/kg of the compound obtained in the Example 3 was orally administered to female beagles aged 8 months (each group consisting of 2 animals) for 4 weeks. This compound was triturated with lactose and administered once a day.
  • the toxicologically non-influential dose of the compound obtained in the Example 3 was judged to be 100 mg/kg.

Abstract

The present invention is a quinone derivative which exhibits excellent therapeutic activity represented by the general formula (I) or a pharmacologically acceptable salt thereof: ##STR1## wherein A stands for a group represented by the formula: ##STR2## (wherein R3, R4 and R5 is the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are each a lower alkoxy group
R1 stands for a heteroarylalkyl group; and
B stands for a carboxyl group or a protected carboxyl group.

Description

FIELD OF THE INVENTION
The present invention relates to a quinone derivative exhibiting an excellent activity as a drug.
BACKGROUND OF THE INVENTION
Among inflammatory mediators, leukotrienes and thromboxanes have recently been noticed. They each cause inflammation alone or interact with each other to cause it, or participate in the continuation of inflammation. However, few compounds exhibiting both leukotrienes production-inhibiting activity and thromboxanes production-inhibiting activity have been found.
The inventors of the present invention have made intensive studies for many years to obtain a compound exhibiting both of the above-mentioned activities and have found that a quinone derivative which will be described below exhibits both the activities at a well-balanced activity ratio and is excellent as a so-called dual inhibitor. The present invention has been accomplished on the basis of this finding.
SUMMARY OF THE INVENTION
The present invention provides a quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR3## wherein A stands for a group represented by the formula: ##STR4## (wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group) or a group represented by the formula: ##STR5## (wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that a case wherein R3 and R4 are each a lower alkoxy group simultaneously is excepted; X and Y are the same or different from each other and each stand for a hydroxyl group or a protected hydroxyl group); R1 stands for a heteroarylalkyl group; and B stands for a carboxyl group or a protected carboxyl group.
Preferably quinone derivatives or pharmacologically acceptable salts thereof of the present invention include derivatives where R1 in the general formula (I) is a heteroarylalkyl group, where R3 in the genaral formula (I) is a lower alkoxy group, where R4 in the general formula (I) is a lower alkyl group, where R5 in the general formula (I) is a lower alkyl group, where X in the general formula (I) is a hydroxy group or a alkoxy group, where Y in the general formula (I) is a hydroxy group or a alkoxy group and where B in the general formula (I) is a carboxyl group.
Still preferably quinone derivatives or pharmacologically acceptable salts thereof of the present invention include derivatives where R1 in the general formula (I) is a pyridylhexyl group or a pyridylpentyl group, where R3 in the general formula (I) is a methoxy group or a methyl group, where R4 in the general formula (I) is a methyl group or a methoxy group, where R5 in the general formula (I) is a methyl group or a methoxy group, where X in the general formula (I) is a hydroxy group or a methoxy group and where Y in the general formula (I) is a hydroxy group or a methoxy group.
The quinone derivative portion of the quinone derivative or pharmacologically acceptable salt thereof of the present invention is advantageously selected from the group consisting of the below listed quinone derivatives:
(E)-3-(2-Methoxy-3,5-dimethyl-1,4-benzoquinon-6-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2-Methoxy-5,6-dimethyl-1,4-benzoquinon-3-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2-Methoxy-5,6-dimethyl-1,4-benzoquinon-3-yl)-2-[6-(3-pyridyl)hexyl]-2-propenoic acid
(E)-3-(2,4,5-Trimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2,5-Dihydroxy-4-methoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2,3,5-Trimethoxy-4,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid.
The quinone derivative portion of the quinone derivative or pharmacologically acceptable salt thereof of the present invention is still advantageously (E)-3-(2-methoxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid.
The present invention also provides leukotrienes production inhibitor and/or thromboxanes production inhibitor comprising a quinone derivative or pharmacologically acceptable salt thereof of the present invention as an active ingredient.
The present invention further provides a therapeutic and preventive agent for diseases for which leukotrienes production inhibitor and/or thromboxanes inhibitor are efficacious, which comprise a quinone derivative or pharmacologically acceptable salt thereof of the present invention as an active ingredient.
The present invention provides a pharmacological composition which comprises a therapeutically effective amount of the quinone derivative or a pharmacologically acceptable salt thereof of the present invention and a pharmacologically acceptable vehicle.
The present invention also provides use of a quinone derivative or a pharmacologically acceptable salt thereof of the present invention for the making of a medicament for treating a disease in which the production of leukotriene is elevated, and/or, a disease in which the production of thromboxane A2 is elevated.
The present invention further provides use of a quinone derivative or a pharmacologically acceptable salt thereof of the present invention for the making of a medicament for treating a disease selected from the group consisting of asthma, chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus, cirrhosis, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency, nephrosis and nephritis.
The present invention provides a method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof of the present invention to a patient suffering from a disease in which the production of leukotriene is elevated, and/or, a patient suffering from a disease in which the production of thromboxane A2 is elevated.
The present invention also provides a method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof of the present invention to a patient suffering from a disease selected from the group consisting of asthma, chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus, cirrhosis, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency, nephrosis and nephritis.
DETAILED DESCRIPTION OF THE INVENTION
The compound of the present invention is a quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR6## wherein A stands for a group represented by the formula: ##STR7## (wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group) or a group represented by the formula: ##STR8## (wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that a case wherein R3 and R4 are each a lower alkoxy group simultaneously is excepted; X and Y are the same or different from each other and each stand for a hydroxyl group or a protected hydroxyl group);
R1 stands for a heteroarylalkyl group; and
B stands for a carboyxl group or a protected carboxyl group.
In the above definition of the compound (I) according to the present invention, the lower alkyl group defined with respect to R3, R4 and R5 is a straight-chain or branched alkyl group having 1 to 8 carbon atoms and examples thereof include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, n-pentyl(amyl) group, isopentyl group, neopentyl group, tert-pentyl group, 1-methylbutyl group, 2-methylbutyl group, 3-methylbutyl, 1,2-dimethylpropyl group, n-hexyl group, isohexyl group, 1-methylpentyl group, 2-methylpentyl group, 3-methylpentyl group, 1,1-dimethylbutyl group, 1,2-dimethylbutyl group, 2,2-dimethylbutyl group, 1,3-dimethylbutyl group, 2,3-dimethylbutyl group, 3,3-dimethylbutyl group, 1-ethylbutyl group, 2-ethylbutyl group, 1,1,2-trimethylpropyl group, 1,2,2-trimethylpropyl group, 1-ethyl-1-methylpropyl group, 1-ethyl-2-methylpropyl group, heptyl group and octyl group. Among these groups, methyl group, ethyl group, n-propyl group and isopropyl group are desirable.
The lower alkoxy group defined with respect to R3, R4 and R5 is one derived from the above-mentioned lower alkyl group and examples thereof include methoxy group, ethoxy group and n-propoxy group, among which a methoxy group is most desirable.
The alkoxy group constituting the alkoxyalkyl group defined with respect to R3, R4 and R5 has 1 to 8 carbon atoms, preferably 1 to 2 carbon atoms, while the alkyl group, i.e., the alkylene chain constituting it has 1 to 10 carbon atoms.
The alkoxyalkoxy group defined with respect to R3 R4 and R5 is one derived from the above-mentioned lower alkoxy group and examples thereof include methoxymethoxy group, methoxyethoxy group, ethoxyethoxy group and methoxypropoxy group.
The cycloalkyl group constituting the cycloalkylalkoxy group defined with respect to R3, R4 and R5 has 3 to 7 carbon atoms, preferably 5 or 6 carbon atoms, while the alkoxy group constituting it is as defined above with respect to the lower alkoxy group.
The alkyl group constituting the thioalkyl group defined with respect to R3, R4 and R5 has 1 to 8 carbon atoms, preferably 1 or 2 carbon atoms.
In the present invention, both R3 and R4 cannot be each a lower alkoxy group such as a methoxy group simultaneously.
The most desirable combination of R3, R4 and R5 is a case wherein one of R3, R4 and R5 is a lower alkoxy group such as a methoxy group and the others are each a lower alkyl group such as a methyl group and ethyl group, which may be the same or different from each other.
The heteroaryl group constituting the heteroarylalkyl group defined with respect to R1 is preferably a 5- or 6-membered nitrogenous heteroaryl group and particular examples thereof include pyridyl group and imidazolyl group, which may be either unsubstituted or each substituted with a lower alkyl group such as a methyl group and ethyl group, a lower alkoxy group such as a methoxy grooup and ethoxy group or a halogen atom such as chlorine atom and bromine atom.
The alkyl group constituting the heteroarylalkyl group, i.e. the alkylene chain has 1 to 10 carbon atoms, preferably 2 to 8 carbon atoms, still preferably 4 to 6 carbon atoms. Further, the alkylene chain may have a substituted lower alkyl group such as a methyl group and ethyl group at any carbon atom.
The protected hydroxyl group defined with respect to X and Y may be, for example, a hydroxyl group protected with the above-mentioned lower alkyl group such as a methyl group and ethyl group, i.e., an alkoxy group, or a hydroxyl group protected with an acyl group such as an acetyl group, propionyl group, butyroyl group, pivaloyl group and nicotinoyl group, i.e., a group having an ester bond. In short, it may be any one which can be deprotected by some means in vivo to regenerate a hydroxyl group.
The protective group constituting the protected carboxyl group defined with respect to B includes lower alkyl groups such as methyl group, ethyl group and t-butyl group; lower alkyl groups substituted with a phenyl group which may be substituted, such as p-methoxybenzyl group, p-nitrobenzyl group, 3,4-dimethoxybenzyl group, diphenylmethyl group, trityl (triphenylmethyl) group and phenethyl group; halogenated lower alkyl groups such as 2,2,2-trichloroethyl group and 2-iodoethyl group; lower alkanoyloxy lower alkyl groups such as pivaloyloxymethyl group, acetoxymethyl group, propionyloxymethyl group, butyryloxymethyl group, valeryloxymethyl group, 1-acetoxyethyl group, 2-acetoxyethyl group, 1-pivaloyloxyethyl group and 2-pivaloyloxyethyl group; higher alkanoyloxy lower alkyl groups such as palmitoyloxyethyl group, heptadecanoyloxymethyl group and 1-palmitoyloxyethyl group; lower alkoxycarbonyloxy lower alkyl groups such as methoxycarbonyloxymethyl group, 1-butoxycarbonyloxyethyl group, 1-t-butoxycarbonyloxyethyl group, 1-ethoxycarbonyloxyethyl group and 1-(isopropoxycarbonyloxy)ethyl group; carboxy lower alkyl groups such as carboxymethyl group and 2-carboxyethyl group; heterocyclic groups such as 3-phthalidyl group; benzoyloxy lower alkyl groups which may be substituted, such as 4-glycyloxybenzoyloxymethyl group and 4-[N-(t-butoxycarbonyl)-glycyloxy]benzoyloxymethyl group; (substituted dioxolene) lower alkyl groups such as (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl group; cycloalkylsubstituted lower alkanoyloxy lower alkyl groups such as 1-cyclohexylacetyloxyethyl group; and cycloalkyloxycarbonyloxy lower alkyl groups such as 1-cyclohexyloxycarbonyloxyethyl group.
Further, the protected carboxyl group may be an acid amide.
In short, the protected carboxyl group may be any one which can be deprotected by some means in vivo to regenerate a carboxyl group.
The pharmacologically acceptable salt according to the present invention includes inorganic acid salts such as hydrochloride, hydrobromide, sulfate and phosphate; organic acid salts such as acetate, maleate, tartrate, methanesulfonate, benzenesulfonate and toluenesulfonate; and amino acid salts such as argininate, aspartate and glutamate.
Further, the quinone derivative of the present invention can form a metal salt such as sodium salt, potassium salt, calcium salt and magnesium salt. The pharmacologically acceptable salt of the present invention includes these metal salts.
Although the compound of the present invention may be present as geometrical isomers (including cis-and trans-isomers) because it has a double bond in its molecule, it is needless to say that the present invention includes all of the isomers.
Representative processes for the preparation of the compound according to the present invention will now be described.
PREPARATION PROCESS 1 ##STR9## (in the above formulas (II) and (III), X, Y, R1, R3, R4, R5 and B are each as defined above).
In the above reaction scheme, the compounds (II) and (III) are compounds of the present invention. As apparent from the reaction scheme, the benzoquinone derivative represented by the formula (III) can be prepared by reacting the hydroquinone derivative represented by the formula (II) with an oxidizing agent, while the hydroquinone derivative (II) can be prepared by the reduction of the benzoquinone derivative (III).
In the oxidation of the hydroquinone derivative represented by the formula (II), for example, cerium (IV) ammonium nitrate, ferric chloride hexahydrate or lead oxide is used as an oxidizing agent. The amount of the oxidizing agent to be used is preferably 2 to 10 times by mole as much as the hydroquinone. The preferable solvent to be used in the oxidation includes acetonitrile, benzene, ethyl acetate, dioxane, ethanol, 1,2-dimethoxyethane and mixtures thereof with water. The oxidation is conducted at a reaction temperature of 0° to 80° C., preferably 0° to 20° C. The reaction time is generally about 1 to 12 hours.
Contrariwise, in reducing the quinone derivative into the hydroquinone derivative which is one of the objective compounds, sodium borohydride or sodium hydrosulfite is preferably used as a reducing agent. The preferable solvent to be used in the reduction includes ethanol, tetrahydrofuran, ethyl acetate, 1,2-dimethoxyethane and mixtures thereof with water. The reaction temperature is preferably 0° to 40° C., still preferably 0° to 20° C.
PREPARATION PROCESS 2
The hydroquinone derivative (II') which is one of the objective compounds according to the present invention can be prepared also by the following process: ##STR10## (in the above reaction scheme, R1, R3, R4, R5, X and Y are each as defined above;
and B' is a group selected from among those defined with respect to B except for a carboxyl group).
More precisely, an objective compound represented by the general formula (II') can be prepared by reacting an aldehyde derivative represented by the general formula (IV) with a phosphonate represented by the general formula (V) in the presence of a base through the Wittig reaction [see, e.g., J.A.C.S., 83, 1733(1961)].
The base to be used in this reaction includes alkali metal hydrides such as sodium hydride and potassium hydride; and alkali metal alcoholates such as sodium methylate, sodium ethylate and potassium tert-butoxide. Preferred examples of the solvent to be used therein include benzene, toluene, dichloromethane, tetrahydrofuran, dioxane, dimethoxyethane and dimethylformamide. The reaction temperature is 0° to 100° C., preferably 20° to 80° C.
PREPARATION PROCESS 3
A hydroquinone derivative represented by the general formula (I) wherein B is a carboxyl group can be prepared by the following process: ##STR11## (in the above reaction scheme, R1, R3, R4, R5, X, Y and B' are each as defined above).
More particularly, a compound represented by the general formula (VI) which is one of the objective compounds can be prepared by saponifying a compound represented by the general formula (II') with an alkali according to the conventional process.
This saponification is conducted by the use of the conventional alkali such as alcoholic caustic soda or potash.
The compound (VI) prepared by this process can be easily oxidized into a compound represented by the general formula (VII) which is one of the objective compounds according to the present invention in a similar manner to that described in the Preparation process 1. ##STR12## (in the above reaction scheme, R1, R3, R4, R5, X and Y are each as defined above).
PREPARATION PROCESS 4
A compound represented by the general formula (I) wherein B is a protected carboxyl group can be prepared by the following process: ##STR13## (in the above reaction scheme, R1, R3, R4, R5 and B' are each as defined above).
When the objective compound (II') or (VIII) is an ester, it can be prepared by esterifying a carboxylic acid represented by the general formula (VII) by the conventional process.
The solvent to be used in this esterification may be any one which is inert to the esterification. The reaction temperature is not particularly limited, but varies depending upon the kind of the reactive derivative.
When the objective compound (II') or (VIII) is an amide, it can be prepared by converting a carboxylic acid represented by the general formula (VII) or a reactive derivative thereof into a corresponding amide by the conventional process.
The reactive derivative of the compound (VII) includes acid halides such as acid chloride and acid bromide; acid azide; active esters thereof with N-hydroxybenzotriazole or N-hydroxysuccinimide; symmetric anhydride; and mixed acid anhydride thereof with alkylcarbonic acid or p-toluenesulfonic acid.
When the compound (VII) is a free carboxylic acid, it is preferable to conduct the amidation of the compound (VII) in the presence of a condensing agent such as dicyclohexylcarbodiimide and 1,1'-carbonyldiimidazole.
The amidation is conducted in an organic solvent inert to the amidation, for example, pyridine, tetrahydrofuran, dioxane, ether, benzene, toluene, xylene, methylene chloride, dichloroethane, chloroform, dimethylformamide, ethyl acetate or acetonitrile.
The reaction temperature is not particularly limited but varies depending upon the kind of the reactive derivative.
The processes for the preparation of the compounds according to the present invention can be illustrated by the following reaction scheme: ##STR14##
Experimental Examples will now be described in order to illustrate the effect of the compounds according to the present invention.
EXPERIMENTAL EXAMPLE Inhibitory activity against the production of leukotriene B4 (LTB4) and thromboxane B2 (TxB2 from rat abdominal infiltration cell METHOD OF EXPERIMENT
10 ml of a 6% (w/v) solution of glycogen (Type II from Oyster, Sigma) in physiological saline was injected into the abdominal cavity of a Fisher male rat having a weight of 150 to 200 g. After 20 to 24 hours, the abdominal exudation cells were recovered therefrom, washed and suspended in the Hanks' balanced salt solution (HBSS) in a concentration of 5×106 /ml. This suspension was poured onto a 96-well culture plate (Costar: registered trademark) in which a test drug diluted to a predetermined concentration had been put in an amount of 10 μl/well, in an amount of 100 μl/well. The resulting plate was incubated at 37° C. for 5 minutes. Calcium ionophore A-23187 [Calbiochem (registered trademark)] was added in a final concentration of 2 μg/ml. After the reaction at 37° C. for additional 10 minutes, the plate was put on ice and a BW755C solution was added in a final concentration of 100 μM. The resulting plate was centrifuged at 15000 rpm for 10 minutes. The supernatant was recovered and the amounts of LTB4 and TxB2 in the supernatant were determined by enzyme immunoassay with an EIA kit mfd. by Cayman.
Results
The inhibitory activities (IC50) of each compound (shown by the number of Example which will be described below) against the production of leukotriene B4 and thromboxane B2 are given in Table 1.
              TABLE 1                                                     
______________________________________                                    
            IC.sub.50 of rat abdominal glycogenic                         
Compound    infiltration cell (μM)                                     
No.         LTB.sub.4   TxB.sub.2                                         
______________________________________                                    
Ex. 9       3.16        0.16                                              
Ex. 3       1.16        0.05                                              
Ex. 6       0.59        0.12                                              
Ex. 4       7.86        0.46                                              
Ex. 5       3.16        0.48                                              
Ex. 7       1.39        0.09                                              
 Ex. 10     0.32        0.42                                              
______________________________________
(Thromboxane A2 is very unstable to treat and naturally turns to thromboxane B2 in 10-20 seconds in the human body. Therefore, thromboxane B2 was used in the tests above).
It can be understood from the results of the above Experimental Examples that the compound of the present invention has an inhibitory activity against the production of both leukotrienes (LTs) and thromboxane (Tx).
Accordingly, the quinone derivatives according to the present invention are efficacious for diseases for which a leukotriene production-inhibiting activity and/or a thromboxane A2 production-inhibiting activity is efficacious. Examples of such diseases include asthma, various liver troubles (such as chronic hepatitis, acute hepatitis, drug-induced hepatitis, viral hepatitis, alcoholic hepatitis, icterus and cirrhosis), ischemic heart diseases (such as myocardial infarction and angina pectoris), cerebral ischemic diseases (such as cerebral embolism and cerebral thrombosis) and various kidney diseases (such as renal insufficiency, nephrosis and nephritis).
Further, the compounds of the present invention are highly safe and therefore are valuable in this respect.
In using the compounds of the present invention as an inhibitor against leucotriene and/or thromboxane production to treat or prevent various diseases, they may be each administered orally as a powder, granule, capsule or syrup, or parenterally as a suppository, injections, external preparation or drop. Although the dose of the compound remarkably varies depending upon the symptom, the age of a patient and the kind of disease, it is generally about 0.1 to 2,000 mg, preferably about 2 to 500 mg, still preferably about 5 to 150 mg per adult a day, which may be administered in one to several portions a day.
The compounds of the present invention can be converted into pharmaceutical preparations by the use of the conventional excipients carriers according to the conventional processes.
A solid preparation for oral administration according to the present invention is prepared by adding a vehicle and, if necessary, a binder, disintegrator, lubricant, colorant and/or corrigent to an active ingredient and shaping the obtained mixture into a tablet, coated tablet, granule, powder or capsule.
Examples of the vehicle include lactose, corn starch, sucrose, glucose, sorbitol, crystalline cellulose and silicon dioxide; those of the binder include polyvinyl alcohol, polyvinyl ether, ethylcellulose, methylcellulose, gum arabic, tragacanth, gelatin, shellac, hydroxypropylcellulose, hydroxylpropylmethylcellulose, calcium citrate, dextrin and pectin; those of the lubricant include magnesium stearate, talc, polyethylene glycol, silica and hardened vegetable oil; those of the colorant include those authorized as pharmaceutical additives; and those of the corrigent include cocoa powder, menthae herba (menthol), aromatic powder, mentha oil (peppermint oil), borneol and powdered cinnamon bark. Of course, the tablet and granule may be suitably coated with sugar, gelatin and the like, if necessary.
An injection according to the present invention is prepared by adding a pH modifier, buffer, stabilizer and/or solubilizing agent to an active ingredient at need and converting the mixture into an injection for subcutaneous, intramuscular or intravenous administration.
EXAMPLE
Examples of the present invention will now be described below, though it is needless to say that the present invention is not limited to them.
The preparation of the starting compounds for preparing the compounds of the present invention will be described in the following Preparative Examples.
The symbols in the chemical formulas which will be given below have the following meaning respectively:
Me: methyl group, Et: ethyl group,
n-Bu: n-butyl group, n-Hep: n-heptyl group,
MOMO: methoxymethoxy group
PREPARATIVE EXAMPLE 1 Ethyl 2-diethylphosphono-7-(3-pyridyl)heptanoate ##STR15##
221 g of 5-(3-pyridyl)pentanol was dissolved in methylene chloride (2 l), followed by the addition of 142 g of triethylamine. Mesyl chloride (161 g) was dropped into the obtained mixture under cooling with ice. After the completion of the dropping, the obtained mixture was stirred for one hour under cooling with ice. The organic layer was washed with water twice, dried over magnesium sulfate and distilled in a vacuum to remove the solvent. A pale-red oil was obtained as a residue.
Separately, sodium hydride (55% oil suspension, 59 g) was suspended in N,N-dimethylformamide (500 ml), followed by the dropwise addition of 300 g of triethyl phosphonoacetate. The obtained mixture was stirred at 50° to 60° C. for one hour, followed by the addition of a solution of the above residue (a pale-red oil) in N,N-dimethylformamide (500 ml). The obtained mixture was stirred at 50° to 60° C. for 18 hours. After the completion of the reaction, ethyl acetate (3 l) was added to the reaction mixture and the mixture was washed with a saturated aqueous solution of sodium chloride twice. The organic layer was dried over anhydrous magnesium sulfate and distilled in a vacuum to remove the solvent. The residue was purified by silica gel column chromatography [n-hexane/ethyl acetate (30%-50%), ethyl acetate-methanol (5%)] to give 226 g of the title compound as a pale-red oil.
EXAMPLE 1 Ethyl (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoate ##STR16##
24 g (0.6 mol) of 60% sodium hydride was suspended in 200 ml of N,N-dimethylformamide and the obtained suspension was stirred at room temperature.
A solution of 222 g (0.6 mol) of the ethyl 2-diethylphosphono-7-(3-pyridyl)heptanoate (a Wittig reagent) prepared in the Preparative Example 1 in 300 ml of N,N-dimethylformamide was gradually dropped into the above suspension. After the completion of the dropping, the obtained mixture was stirred at room temperature for one hour to give a transparent solution. A solution of 122 g (0.54 mol) of 2,4,5-trimethoxy-3,6-dimethylbenzaldehyde in 200 ml of N,N-dimethylformamide was dropped into the transparent solution. The obtained mixture was stirred overnight under heating at 50° C.
The reaction mixture was poured onto 1 l of ice-water. The obtained mixture was extracted with 1 l of ethyl acetate twice. The organic layer was dried over magnesium sulfate and distilled to remove the solvent. The residue was subjected to silica gel column chromatography [solvent: n-hexane→ethyl acetate (10%→30%)/n-hexane].
177 g of the title compound was obtained as a pale-yellow oil.
1 H-NMR (400 MHz, CDCl3) δ (ppm); 1.21 (tt, J=7.5, 7.5 Hz, 2H), 1.35 (t, J=7.1 Hz, 3H), 1.38 (tt, J=7.5, 7.5 Hz, 2H), 1.46 (tt, J=7.5, 7.5 Hz, 2H), 2.07 (s, 3H), 2.16 (t, J=7.5 Hz, 2H), 2.16 (s, 3H), 2.48 (t, J=7.5 Hz, 2H), 3.54 (s, 3H), 3.76 (s, 3H), 3.82 (s, 3H), 4.12 (q, J=7.1 Hz, 2H), 7.16 (dd, J=5.5, 7.8 Hz, 1H), 7.39 (dt, J=1.5, 5.5 Hz, 1H), 7.45 (s, 1H), 8.36 (d, J=1.5 Hz, 1H), 8.39 (dd, J=1.5, 5.5 Hz, 1H).
EXAMPLE 2 (E)- 3-(2,4,5-Trimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid ##STR17##
177 g (0.39 mol) of the ester prepared in Example 1 was dissolved in 500 ml of ethanol, followed by the addition of 100 ml of an aqueous solution of 78 g of sodium hydroxide. The obtained mixture was heated under reflux for one hour, followed by the addition of 1 l of ice. The obtained mixture was neutralized with 6N hydrochloric acid. The resulting mixture was extracted with 1 l of ethyl acetate twice. The organic layer was washed with an aqueous solution of sodium chloride, dried over magnesium sulfate and distilled to remove the solvent. 159 g of the title compound was obtained as a colorless oil.
1 H-NMR (400 MHz, CDCl3) δ (ppm); 1.24 (tt, J=7.6, 7.6 Hz, 2H), 1.47 (tt, J=7.6, 7.6 Hz, 2H), 1.52 (tt, J=7.6, 7.6 Hz, 2H), 2.09 (s, 3H), 2.17 (s, 3H), 2.20 (t, J=7.6 Hz, 2H), 2.54 (t, J=7.6 Hz, 2H), 3.57 (s, 3H), 3.78 (s, 3H), 3.83 (s, 3H), 7.23 (dd, J=5.0, 7.6 Hz, 1H), 7.48 (bd, J=7.6 Hz, 1H), 7.59 (s, 1H), 8.46 (bs, 2H).
EXAMPLE 3
(1) (E)-3-(2-Methoxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid ##STR18##
159 g (0.39 mol) of the carboxylic acid prepared in the Example 2 was dissolved in an acetonitrile (800 ml)/water (400 ml) mixture. The obtained solution was cooled in an ice bath, followed by the gradual dropwise addition of 700 ml of an aqueous solution of 527 g (0.96 mol) of cerium (IV) ammonium nitrate. The obtained mixture was stirred for 30 minutes and the pH thereof was adjusted to 5 with a saturated solution of sodium hydrogencarbonate, followed by the addition of 3 l of water. The obtained mixture was extracted with 6 l of ethyl acetate twice. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and distilled to remove the solvent. The obtained oil was crystallized from a small amount of ethyl acetate to give 114 g of a yellow crystal. This crystal was recrystallized from an ethanol/water mixture to give 90 g of the title compound.
m.p.: 134° to 135° C.
1 H-NMR (400 MHz, CDCl3) δ (ppm); 1.26 (tt, J=7.0, 7.0 Hz, 2H), 1.50 (tt, J=7.0, 7.0 Hz, 2H), 1.61 (tt, J=7.0, 7.0 Hz, 2H), 1.95 (s, 3H), 1.96 (s, 3H), 2.12 (t, J=7.0 Hz, 2H), 2.60 (t, J=7.0 Hz, 2H), 4.01 (s, 3H), 7.26 (s, 1H), 7.27 (dd, J=5.0, 8.5 Hz, 1H), 7.55 (bd, J=8.5 Hz, 1H), 8.44 (bd, J=5.0 Hz, 1H), 8.50 (bs, 1H).
(2) (E)-3-(2-Methoxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid hydrochloride ##STR19##
A hydrochloride of the compound described above (1) was prepared by the conventional process.
m.p.: 138° to 139° C.
1 H-NMR (400 MHz, DMSO-d6) δ (ppm); 1.18 (tt, J=7.2, 7.2 Hz, 2H), 1.37 (tt, J=7.2, 7.2 Hz 2H), 1.54 (tt, J=7.2, 7.2 Hz, 2H), 1.82 (s, 3H), 1.84 (s, 2H), 2.04 (t, J=7.2 Hz, 2H), 2.71 (t, J=7.2 Hz, 2H), 3.92 (s, 3H), 7.04 (d, J=1.2 Hz, 1H), 7.97 (dd, J=2.4, 8.0 Hz, 1H), 8.41 (d, J=8.0 Hz, 1H), 8.76 (d, J=5.6 Hz, 1H), 8.79 (s, 1H).
EXAMPLE 4 (E)-3-(2,5-Dihydroxy-4-methoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid ##STR20##
1.0 g of the quinone prepared in the Example 3 (1) was suspended in 150 ml of ethyl acetate and the obtained suspension was fully mixed with a solution of 2 g of sodium hydrosulfite in 50 ml of water. The organic layer was separated, dried over anhydrous magnesium sulfate and concentrated in a vacuum to give 660 mg of the title compound as a white amorphous substance.
1 H-NMR (400 MHz, CDCl3) δ (ppm); 1.21 (tt, J=7.0, 7.0 Hz, 2H), 1.44 (tt, J=7.0, 7.0 Hz, 2H), 1.51 (tt, J=7.0, 7.0 Hz, 2H), 2.06 (s, 3H), 2.17 (s, 3H), 2.23 (t, J=7.0 Hz, 2H), 2.54 (t, J=7.0 Hz, 2H), 3.76 (s, 3H), 5.22 (bs, 2H), 7.26 (dd, J=5.5, 7.0 Hz, 1H), 7.43 (s, 1H), 7.51 (dd, J=1.5, 7.0 Hz, 1H), 8.40-8.47 (m, 2H).
EXAMPLES 5 TO 22
The compounds listed in the following Tables 2 to 7 were each prepared in a similar manner to that of the Example 1.
                                  TABLE 2                                 
__________________________________________________________________________
 ##STR21##                                                                
Ex.                    .sup.1 H-NMR spectrum                              
No.                                                                       
   R.sup.3                                                                
        R.sup.4                                                           
            R.sup.5                                                       
               n Properties                                               
                       TMS as internal reference, δ value           
__________________________________________________________________________
                       (ppm)                                              
5  n-HepO                                                                 
        Me  Me 5 colorless                                                
                       0.90 (t, J=7.0Hz, 3H), 1.16-1.58 (m, 14H), 1.26    
                       (t, J=7.0Hz, 3H), 1.76 (tt, J=7.0,                 
                 oil   7.0Hz, 2H), 2.07 (s, 3H), 2.08-2.20 (m, 2H), 2.17  
                       (s, 3H), 2.48 (t, J=7.0Hz, 2H), 3.54               
                       (s, 3H), 3.75 (s, 3H), 3.91 (t, J=7.0Hz, 2H), 4.27 
                       (q, J=7.0Hz, 2H), 7.18                             
                       (dd, J=5.0, 8.0Hz, 1H), 7.40 (bd, J=8.0Hz, 1H),    
                       7.46 (s, 1H), 8.38 (d, J=1.5Hz,                    
                       1H), 8.40 (bd, J=5.0Hz, 1H)                        
6  Me   MeO Me 5 colorless                                                
                       1.21 (tt, J=8.0, 8.0Hz, 2H), 1.35 (t, J=7.2Hz,     
                       3H), 1.40 (t, J=8.0Hz, 2H), 1.48 (tt,              
                 oil   J=8.0, 8.0Hz, 2H), 2.07 (s, 3H), 2.15 (t, J=8.0Hz, 
                       2H), 2.21 (s, 3H), 2.49 (t, J=8.0Hz,               
                       2H), 3.65 (s, 3H), 3.70 (s, 3H), 3.77 (s, 3H),     
                       4.28 (q, J=7.2Hz, 2H), 7.16 (dd, J=4.8,            
                       7.6Hz, 1H), 7.39 (d, J=8.0Hz, 1H), 7.44 (s, 1H),   
                       8.36 (d, J=1.6Hz, 1H), 8.40 (dd, J=                
                       1.6, 4.8Hz, 1H)                                    
7  Me   n-BuO                                                             
            Me 5 colorless                                                
                       0.97 (t, J=8.0Hz, 3H), 1.22 (tt, J=7.6Hz, 2H),     
                       1.36 (t, J=8.0Hz, 3H), 1.38-1.52 (m,               
                 oil   6H), 1.725 (tt, J=7.6, 7.6Hz, 2H), 2.06 (s, 3H),   
                       2.15 (t, J=7.6Hz, 2H), 2.20 (s, 3H),               
                       2.48 (t, J=7.6Hz, 2H), 3.65 (s, 3H), 3.67 (s, 3H), 
                       3.88 (t, J=8.0Hz, 2H), 4.275 (q,                   
                       J=8.0Hz, 2H), 7.17 (dd, J=4.8, 7.6Hz, 1H), 7.39    
                       (d, J=7.6Hz, 1H), 7.45 (s, 1H), 8.36               
                       (s, 1H), 8.41 (d, J=4.8Hz, 1H)                     
__________________________________________________________________________

                                  TABLE 3                                 
__________________________________________________________________________
 ##STR22##                                                                
Ex.                   .sup.1 H-NMR spectrum                               
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
           R.sup.5                                                        
              n Properties                                                
                      TMS as internal reference, δ value            
__________________________________________________________________________
                      (ppm)                                               
8  Me n-BuO                                                               
           Me 3 colorless                                                 
                      0.98 (t, J=8.0Hz, 3H), 1.34 (t, J=8.0Hz, 3H), 1.51  
                      (q, J=7.6Hz, 2H), 1.67-1.80 (m, 4H),                
                oil   2.06 (s, 3H), 2.20 (t, J=7.6Hz, 2H), 2.23 (s, 3H),  
                      2.47 (t, J=7.6Hz, 2H), 3.67 (s, 6H),                
                      3.89 (t, J=8.0H, 2H), 4.27 (q, J=8.0Hz, 2H), 7.09   
                      (dd, J=4.8, 7.6Hz, 1H), 7.32 (d, J=                 
                      7.6Hz, 1H), 7.48 (s, 1H), 8.31 (s, 1H), 8.37 (d,    
                      J=4.8Hz, 1H)                                        
9  Me n-HepO                                                              
           Me 5 colorless                                                 
                      0.89 (t, J=7.0Hz, 3H), 1.21 (tt, J=8.0, 8.0Hz, 2H), 
                      1.25-1.52 (m, 12H), 1.35 (t, J=7.5Hz,               
                oil   3H), 1.74 (tt, J=8.0, 8.0Hz, 2H), 2.07 (s, 3H),     
                      2.15 (t, J=8.0Hz, 2H), 2.21 (s, 3H), 2.48           
                      (t, J=8.0Hz, 2H), 3.66 (s, 3H), 3.68 (s, 3H), 3.88  
                      (t, J=6.5Hz, 2H), 4.27 (q, J=7.5Hz,                 
                      2H), 7.16 (dd, J=4.8, 7.5Hz, 1H), 7.39 (d, J=7.5Hz, 
                      1H), 7.45 (s, 1H), 8.36 (d, J=                      
                      1.2Hz, 1H), 8.41 (dd, J=1.2, 4.8Hz, 1H)             
10 MeO                                                                    
      Me   Me 3 colorless                                                 
                      1.34 (t, J=7.1Hz, 3H), 1.70 (tt, J=7.6, 7.6Hz, 2H), 
                      2.06 (s, 3H), 2.16 (s, 3H), 2.20 (t,                
                oil   J=7.6Hz, 2H), 2.48 (t, J=7.6Hz, 2H), 3.54 (s, 3H),  
                      3.78 (s, 3H), 3.86 (s, 3H), 4.27 (q,                
                      J=7.1Hz, 2H), 7.11 (dd, J=4.8, 8.0Hz, 1H), 7.33 (d, 
                      J=8.0Hz, 1H), 7.49 (s, 1H), 8.32                    
                      (d, J=2.0Hz, 1H), 8.37 (dd, J=2.0, 4.8Hz,           
__________________________________________________________________________
                      1H)                                                 

                                  TABLE 4                                 
__________________________________________________________________________
 ##STR23##                                                                
Ex.                 .sup.1 H-NMR spectrum                                 
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                    TMS as internal reference, δ value              
__________________________________________________________________________
                    (ppm)                                                 
11 Me Me MeO                                                              
            5 colorless                                                   
                    1.30 (tt, J=7.6, 7.6Hz, 2H), 1.42-1.57 (m, 4H), 2.15  
                    (s, 3H), 2.19 (s, 3H), 2.28 (t, J=7.6Hz,              
              oil   2H), 2.64 (t, J=7.6Hz, 2H), 3.56 (s, 3H), 3.72 (s,    
                    3H), 3.76 (s, 3H), 7.24 (m, 1H), 7.49 (d, J=          
                    7.2Hz, 1H), 7.64 (s, 1H), 8.43 (bs, 2H)               
12 MeO                                                                    
      Me Me 4 colorless                                                   
                    1.33 (t, J=7.2Hz, 3H), 1.41 (tt, J=7.2, 7.2Hz, 2H),   
                    1.49 (tt, J=7.2, 7.2Hz, 2H), 2.06 (s, 3H),            
              oil   2.17 (s, 3H), 2.21 (t, J=7.2Hz, 2H), 2.47 (t,         
                    J=7.2Hz, 2H), 3.52 (s, 3H), 3.77 (s, 3H), 3.84        
                    (s, 3H), 4.27 (q, J=7.2Hz, 2H), 7.15 (dd, J=4.8,      
                    8.0Hz, 1H), 7.37 (d, J=8.0Hz, 1H), 7.47 (s,           
                    1H), 8.35 (d, J=1.6Hz, 1H), 8.39 (dd, J=1.6, 4.8Hz,   
                    1H)                                                   
13 MeO                                                                    
      Me Me 6 colorless                                                   
                    1.19 (t, J=3.2Hz, 4H), 1.35 (t, J=7.0Hz, 5H), 1.51    
                    (t, J=8.0Hz, 2H), 2.08 (s, 3H), 2.16                  
              oil   (t, J=8.0Hz, 2H), 2.17 (s, 3H), 2.52 (t, J=8.0Hz,     
                    2H), 3.55 (s, 3H), 3.78 (s, 3H), 3.85 (s, 3H),        
                    4.27 (q, J=7.0Hz, 2H), 7.19 (dd, J=4.8, 7.6Hz, 1H),   
                    7.44 (d, J=7.6Hz, 1H), 7.46 (s, 1H), 8.40             
                    (s, 1H), 8.42 (d, J=4.8Hz, 1H)                        
__________________________________________________________________________

                                  TABLE 5                                 
__________________________________________________________________________
 ##STR24##                                                                
Ex.                 .sup.1 H-NMR spectrum                                 
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                    TMS as internal reference, δ value              
__________________________________________________________________________
                    (ppm)                                                 
14 Me MeO                                                                 
         Me 6 colorless                                                   
                    1.71-1.23 (m, 4H), 1.33 (t, J=8.0Hz, 5H), 1.51 (tt,   
                    J=8.0, 8.0Hz, 2H), 2.07 (s, 3H), 2.12 (t,             
              oil   J=8.0Hz, 2H), 2.21 (s, 3H), 2.51 (t, J=8.0Hz, 2H),    
                    3.66 (s, 3H), 3.69 (s, 3H), 3.80 (s, 3H),             
                    4.27 (q, J=8.0Hz, 2H), 7.18 (dd, J=4.8, 7.6Hz, 1H),   
                    7.43 (d, J=7.6Hz, 1H), 7.46 (s, 1H), 8.38             
                    (s, 1H), 8.41 (d, J=4.8Hz, 1H)                        
15 Me Me MeO                                                              
            6 colorless                                                   
                    1.21-1.25 (m, 4H), 1.34 (t, J=8.0Hz, 3H), 1.41 (tt,   
                    J=8.0, 8.0Hz, 2H), 1.55 (tt, J=8.0, 8.0Hz,            
              oil   2H), 2.15 (s, 3H), 2.20 (s, 3H), 2.27 (t, J=8.0Hz,    
                    2H), 2.53 (t, J=8.0Hz, 2H), 3.57 (s, 3H),             
                    3.72 (s, 3H), 3.77 (s, 3H), 4.28 (q, J=8.0Hz, 2H),    
                    7.20 (dd, J=4.8, 7.6Hz, 1H), 7.46 (d, J=              
                    7.6Hz, 1H), 7.51 (s, 1H), 8.40 (s, 1H), 8.43 (d,      
                    J=4.8Hz, 1H)                                          
16 H  Me MeO                                                              
            5 colorless                                                   
                    1.25 (t, J=8.0Hz, 2H), 1.35 (t, J=9.0Hz, 3H),         
                    1.40-1.53 (m, 4H), 2.24 (s, 3H), 2.27 (t,             
              oil   J=8.0Hz, 2H), 2.50 (t, J=8.0Hz, 2H), 3.56 (s, 3H),    
                    3.68 (s, 3H), 3.83 (s, 3H), 4.28 (q, J=               
                    9.0Hz, 2H), 6.70 (s, 1H), 7.16 (dd, J=5.0, 9.0Hz,     
                    1H), 7.42 (bd, J=9.0Hz, 1H), 7.51 (s, 1H),            
                    8.36 (bs, 1H), 8.40 (bd, J=5.0Hz, 1H)                 
__________________________________________________________________________

                                  TABLE 6                                 
__________________________________________________________________________
 ##STR25##                                                                
Ex.                        .sup.1 H-NMR spectrum                          
No.                                                                       
   R.sup.3                                                                
      R.sup.4   R.sup.5                                                   
                   n Properties                                           
                           TMS as internal reference, δ value       
__________________________________________________________________________
                           (ppm)                                          
17 Me Me        Me 5 colorless                                            
                           1.17-1.52 (m, 6H), 1.33 (t, J=7.2Hz, 3H), 2.00 
                           (s, 3H), 2.15 (s, 3H), 2.19 (s,                
                     oil   3H), 2.12-2.22 (m, 2H), 2.46 (t, J=7.0Hz, 2H), 
                           3.53 (s, 3H), 3.63 (s, 3H),                    
                           4.26 (q, J=7.2Hz, 2H), 7.16 (dd, J=4.0, 7.6Hz, 
                           1H), 7.38 (dt, J=1.6, 7.6Hz,                   
                           1H), 7.50 (s, 1H), 8.35 (d, J=1.6Hz, 1H), 8.40 
                           (dd, J=1.6, 4.0Hz, 1H)                         
18 Me                                                                     
       ##STR26##                                                          
                Me 5 colorless oil                                        
                           1.12 (dq, J=4.0, 12.0Hz, 2H), 1.16-1.30 (m,    
                           4H), 1.34 (t, J=8.0Hz, 3H), 1.40 (t, J=8.0,    
                           2H), 1.48 (tt, J=8.0, 8.0Hz, 2H), 1.66-1.80    
                           (m, 5H), 1.88 (bd, J= 12.0Hz, 2H), 2.07 (s,    
                           3H), 2.15 (t, J=8.0Hz, 2H), 2.21 (s, 3H), 2.48 
                           (t, J= 8.0Hz, 2H), 3.66 (s, 3H), 3.67 (d,      
                           J=16Hz, 2H), 3.68 (s, 3H), 4.28 (q, J= 8.0Hz,  
                           2H), 7.16 (dd, J=4.8, 7.6Hz, 1H), 7.39 (d,     
                           J=7.6Hz, 1H), 7.45 (s, 1H), 8.37 (d, J=1.6Hz,  
                           1H), 8.41 (dd, J=1.6, 4.8Hz, 1H)               
19 EtO                                                                    
      Me        Me 5 colorless                                            
                           1.20 (m, 2H), 1.30-1.40 (m, 10H), 2.06 (s,     
                           3H), 2.14-2.20 (2, 5H), 2.46 (t, J=            
                     oil   8.0Hz, 2H), 3.53 (s, 3H), 3.74 (s, 3H), 4.00   
                           (q, J=7.0Hz, 2H), 4.26 (q, J=                  
                           7.0Hz, 2H), 7.13 (s, 1H), 7.37 (d, J=8.0Hz,    
                           1H), 7.48 (s, 1H), 8.35 (bs,                   
__________________________________________________________________________
                           2H)                                            

                                  TABLE 7                                 
__________________________________________________________________________
 ##STR27##                                                                
Ex.                       .sup.1 H-NMR spectrum                           
No.                                                                       
   R.sup.3                                                                
        R.sup.4                                                           
               R.sup.5                                                    
                  n Properties                                            
                          TMS as internal reference, δ value        
__________________________________________________________________________
                          (ppm)                                           
20 Me                                                                     
         ##STR28##                                                        
               Me 5 colorless oil                                         
                          1.19 (tt, J=7.5, 7.5Hz, 2H), 1.30-1.35 (m, 5H), 
                          1.45 (tt, J=7.5, 7.5Hz, 2H), 1.73 (t, J=8.0Hz,  
                          2H), 2.08 (s, 3H), 2.15 (t, J=7.5Hz, 2H), 3.33  
                          (s, 3H), 3.40 (t, J= 8.0Hz, 2H), 3.55 (s, 3H),  
                          3.63 (s, 3H), 4.27 (q, J=7.5Hz, 2H), 7.16 (dd,  
                          J= 4.8, 8.0Hz, 1H), 7.37 (d, J=8.0Hz, 1H), 7.50 
                          (s, 1H), 8.35 (s, 1H), 8.40 (d, J=4.8Hz, 1H)    
21 MeS  Me     Me 5 pale-yellow                                           
                          1.22 (tt, J=7.5, 7.5Hz, 2H), 1.32 (t, J=8.0Hz,  
                          3H), 1.39 (tt, J=7.5, 7.5Hz, 2H),               
                    oil   1.47 (tt, J=7.5, 7.5Hz, 2H), 2.11 (s, 3H), 2.14 
                          (t, J=7.5Hz, 2H), 2.38 (s, 3H),                 
                          2.42 (s, 3H), 2.49 (t, J=7.5Hz, 2H), 3.55 (s,   
                          3H), 3.78 (s, 3H), 4.27 (q, J=                  
                          8.0Hz, 2H), 7.17 (dd, J=4.5, 7.5 Hz, 1H), 7.39  
                          (d, J=7.5Hz, 1H), 7.46 (s, 1H),                 
                          8.37 (s, 1H), 8.40 (d, J=4.5Hz, 1H)             
22 MOMO Me     Me 5 pale-yellow                                           
                          1.20 (tt, J=8.0, 8.0Hz, 2H), 1.32 (t, J=8.5Hz,  
                          3H), 1.33 (tt, J=8.0, 8.0 Hz, 2H),              
                    oil   1.48 (tt, J=8.0, 8.0Hz, 2H), 2.05 (s, 3H), 2.16 
                          (t, J=8.0Hz, 2H), 2.22 (s, 3H),                 
                          2.49 (t, J=8.0Hz, 2H), 3.53 (s, 3H), 3.60 (s,   
                          3H), 3.72 (s, 3H), 4.26 (t, J=8.5Hz,            
                          2H), 5.08 (s, 2H), 7.16 (dd, J=4.5, 7.5Hz, 1H), 
                          7.40 (bd, J=7.5Hz, 1H), 7.46                    
                          (s, 1H), 8.35 (bs, 1H), 8.40 (d, J=4.5Hz,       
__________________________________________________________________________
                          1H)
EXAMPLE 23 Ethyl (E)-3-(2-methoxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[6-(3-pyridyl)hexyl]-2-propenoate hydrochloride ##STR29##
0.60 g of the ethyl (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[6-(3-pyridyl)hexyl]-2-propenoate prepared in the Example 13 was dissolved in an acetonitrile (20 ml)/water (10 ml) mixture. The obtained solution was stirred under cooling with ice, followed by the addition of 1.66 g of cerium (IV) ammonium nitrate in portions. The obtained mixture was stirred under cooling with ice for 3 hours, followed by the addition of 100 ml of ethyl acetate. The obtained mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate twice and thereafter with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and filtered. The filtrate was concentrated to 10 ml, adsorbed on a silica gel column and eluted with an ethyl acetate/n-hexane (1:1) mixture. The fractions containing the objective compound were combined and dry hydrogen chloride gas was bubbled thereinto for one minute. The solvent was distilled away in a vacuum. 0.40 g of the title compound was obtained as a yellow oil.
1 H-NMR (DMSO-d6) δ (ppm); 1.07-1.33 (m, 6H), 1.23 (t, J=7.0 Hz, 3H), 1.45-1.57 (t, J=8.0 Hz, 2H), 1.80 (s, 3H), 1.81 (s, 3H), 2.03 (t, J=8.0 Hz, 2H), 2.49 (t, J=8.0 Hz, 2H), 3.91 (s, 3H), 4.18 (q, J=7.0 Hz, 2H), 7.03 (s, 1H), 7.93 (bt, J=8.0 Hz, 1H), 8.37 (bd, J=8.0 Hz, 1H), 8.73 (d, J=8.0 Hz, 1H), 8.76 (s, 1H).
EXAMPLES 24 TO 41
The compounds listed in the following Tables 8 to 13 were each prepared in a similar manner to that of the Example 2:
                                  TABLE 8                                 
__________________________________________________________________________
 ##STR30##                                                                
Ex.                  .sup.1 H-NMR spectrum                                
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
          R.sup.5                                                         
             n Properties                                                 
                     TMS as internal reference, δ value             
__________________________________________________________________________
                     (ppm)                                                
24 MeO                                                                    
      Me  Me 5 colorless                                                  
                     1.24 (tt, J=7.6, 7.6Hz, 2H), 1.47 (tt, J=7.6, 7.6Hz, 
                     2H), 1.52 (tt, J=7.6, 7.6Hz, 2H), 2.09               
               oil   (s, 3H), 2.17 (s, 3H), 2.20 (t, J=7.6Hz, 2H), 2.54   
                     (t, J=7.6Hz, 2H), 3.57 (s, 3H), 3.78 (s,             
                     3H), 3.83 (s, 3H), 7.28 (dd, J=5.0, 7.6Hz, 1H), 7.48 
                     (bd, J=7.6Hz, 1H), 7.59 (s, 1H),                     
                     8.46 (bs, 2H)                                        
25 Me MeO Me 5 colorless                                                  
                     1.21 (tt, J=8.0, 8.0Hz, 2H), 1.35 (t, J=7.2Hz, 3H),  
                     1.40 (t, J=8.0Hz, 2H), 1.48 (tt, J=8.0,              
               oil   8.0Hz, 2H), 2.07 (s, 3H), 2.15 (t, J=8.0Hz, 2H),     
                     2.21 (s, 3H), 2.49 (t, J=8.0Hz, 2H), 3.65            
                     (s, 3H), 3.70 (s, 3H), 3.77 (s, 3H), 4.28 (q,        
                     J=7.2Hz, 2H), 7.16 (dd, J=4.8, 7.6Hz, 1H),           
                     7.39 (d, J=8.0Hz, 1H), 7.44 (s, 1H), 8.36 (d,        
                     J=1.6Hz, 1H), 8.40 (dd, J=1.6, 4.8Hz, 1H)            
26 Me n-BuO                                                               
          Me 5 colorless                                                  
                     0.96 (t, J=8.0Hz, 3H), 1.13 (bs, 2H), 1.40-1.55 (m,  
                     4H), 1.71 (tt, J=7.6, 7.6Hz, 2H), 2.05               
               oil   (s, 3H), 2.13 (t, J=7.6Hz, 2H), 2.19 (s, 3H), 2.48   
                     (t, J=7.6Hz, 2H), 3.62 (bs, 6H), 3.86 (t,            
                     J=8.0Hz, 2H), 7.17 (d, J=7.6Hz, 1H), 7.40 (d,        
                     J=7.6Hz, 1H), 7.51 (s, 1H), 8.44 (s,                 
__________________________________________________________________________
                     2H)                                                  

                                  TABLE 9                                 
__________________________________________________________________________
 ##STR31##                                                                
Ex.                   .sup.1 H-NMR spectrum                               
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
           R.sup.5                                                        
              n Properties                                                
                      TMS as internal reference, δ value            
__________________________________________________________________________
                      (ppm)                                               
27 Me n-BuO                                                               
           Me 3 colorless                                                 
                      0.98 (t, J=8.0Hz, 3H), 1.51 (q, J=7.6Hz, 2H),       
                      1.71-1.85 (m, 4H), 2.04 (s, 3H), 2.22 (bs,          
                oil   5H), 2.52 (t, J=7.6Hz, 2H), 3.66 (s, 6H), 3.90 (t,  
                      J=8.0Hz, 2H), 7.16 (bs, 1H), 7.39 (d,               
                      J=7.6Hz, 1H), 7.56 (s, 1H), 8.42 (bs, 1H), 8.51     
                      (bs, 1H)                                            
28 Me n-HepO                                                              
           Me 5 colorless                                                 
                      0.90 (t, J=8.0Hz, 3H), 1.20-1.38 (m, 10H),          
                      1.41-1.54 (m, 4H), 1.76 (tt, J=7.6, 7.6Hz,          
                oil   2H), 2.08 (s, 3H), 2.18 (t, J=7.6Hz, 2H), 2.21 (s,  
                      3H), 2.53 (t, J=7.6Hz, 2H), 3.67 (s,                
                      3H), 3.69 (s, 3H), 3.90 (t, J=8.0Hz, 3H), 7.23 (t,  
                      J=7.6Hz, 1H), 7.47 (d, J=7.6Hz, 1H),                
                      7.58 (s, 1H), 8.46 (bs, 2H)                         
29 Me EtO  Me 5 colorless                                                 
                      1.24 (tt, J=8.0, 8.0Hz, 2H), 1.35 (t, J=8.0Hz, 3H), 
                      1.40-1.52 (m, 4H), 2.08 (s, 3H), 2.18               
                oil   (t, J=8.0Hz, 2H), 2.21 (s, 3H), 2.53 (t, J=8.0Hz,   
                      2H), 3.66 (s, 3H), 3.69 (s, 3H), 3.99 (q,           
                      J=8.0Hz, 2H), 7.24 (dd, J=4.8, 7.6Hz, 1H), 7.49 (d, 
                      J=7.6Hz, 1H), 7.58 (s, 1H), 8.43                    
                      (s, 1H), 8.46 (s, 1H)                               
__________________________________________________________________________

                                  TABLE 10                                
__________________________________________________________________________
 ##STR32##                                                                
Ex.                 .sup.1 H-NMR spectrum                                 
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                    TMS as internal reference, δ value              
__________________________________________________________________________
                    (ppm)                                                 
30 MeO                                                                    
      Me Me 3 colorless                                                   
                    1.84 (tt, J=7.6, 7.6Hz, 2H), 2.10 (s, 3H), 2.23 (s,   
                    3H), 2.25 (t, J=7.6Hz, 2H), 2.57 (t, J=               
              oil   7.6Hz, 2H), 3.56 (s, 3H), 3.80 (s, 3H), 3.87 (s, 3H), 
                    7.21 (t, J=7.6Hz, 1H), 7.46 (d, J=                    
                    7.6Hz, 1H), 7.60 (s, 1H), 8.46 (bs, 1H), 8.58 (bs,    
                    1H)                                                   
31 Me Me MeO                                                              
            5 colorless                                                   
                    1.30 (tt, J=7.6, 7.6Hz, 2H), 1.42-1.52 (m, 4H), 2.15  
                    (s, 3H), 2.19 (s, 3H), 2.28 (t, J=                    
              oil   7.6Hz, 2H), 2.64 (t, J= 7.6Hz, 2H), 3.56 (s, 3H),     
                    3.72 (s, 3H), 3.76 (s, 3H), 7.24 (m, 1H), 7.49        
                    (d, J=7.2Hz, 1H), 7.64 (s, 1H), 8.43 (bs, 2H)         
32 MeO                                                                    
      Me Me 4 colorless                                                   
                    1.41-1.58 (m, 4H), 2.08 (s, 3H), 2.18 (s, 3H), 2.25   
                    (t, J=7.2Hz, 2H), 2.53 (t, J=7.2Hz, 2H),              
              oil   3.55 (s, 3H), 3.78 (s, 3H), 3.85 (s, 3H), 7.21 (t,    
                    J=7.6Hz, 1H), 7.44 (d, J=7.6Hz, 1H), 7.59             
                    (s, 1H), 8.44 (bs, 2H)                                
__________________________________________________________________________

                                  TABLE 11                                
__________________________________________________________________________
 ##STR33##                                                                
Ex.                 .sup.1 H-NMR spectrum                                 
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                    TMS as internal reference, δ value              
__________________________________________________________________________
                    (ppm)                                                 
33 MeO                                                                    
      Me Me 6 colorless                                                   
                    1.22 (t, J=3.5Hz, 4H), 1.41 (t, J=7.6Hz, 2H), 1.53    
                    (t, J=7.6Hz, 2H), 2.10 (s, 3H), 2.18 (s,              
              oil   3H), 2.19 (t, J=7.6Hz, 2H), 2.55 (t, J=7.6Hz, 2H),    
                    3.57 (s, 3H), 3.79 (s, 3H), 3.85 (s, 3H),             
                    7.23 (t, J=8.0Hz, 1H), 7.51 (d, J=8.0Hz, 1H), 7.58    
                    (s, 1H), 8.47 (bs, 2H)                                
34 Me MeO                                                                 
         Me 6 colorless                                                   
                    1.20-1.27 (m, 4H), 1.42 (tt, J=8.0, 8.0Hz, 2H), 1.55  
                    (tt, J=8.0, 8.0Hz, 2H), 2.11 (s, 3H),                 
              oil   2.19 (t, J=8.0Hz, 2H), 2.23 (s, 3H), 2.58 (t,         
                    J=8.0Hz, 3H), 3.69 (s, 3H), 3.71 (s, 3H),             
                    3.82 (s, 3H), 7.26 (d, J=7.6Hz, 1H), 7.54 (d,         
                    J=7.6Hz, 1H), 7.58 (s, 1H), 8.50 (bs, 2H)             
35 H  Me MeO                                                              
            5 colorless                                                   
                    1.28 (t, J=8.0Hz, 2H), 1.30-1.55 (m, 4H), 2.25 (s,    
                    3H), 2.30 (t, J=8.0Hz, 2H), 2.53 (t, J=               
              oil   8.0Hz, 2H), 3.58 (s, 3H), 3.68 (s, 3H), 3.83 (s, 3H), 
                    6.60 (s, 1H), 7.21 (dd, J=5.0, 7.0Hz, 1H),            
                    7.47 (dd, J=1.0, 9.0Hz, 1H), 7.64 (s, 1H), 8.43 (bs,  
                    2H)                                                   
__________________________________________________________________________

                                  TABLE 12                                
__________________________________________________________________________
 ##STR34##                                                                
Ex.                        .sup.1 H-NMR spectrum                          
No.                                                                       
   R.sup.3                                                                
      R.sup.4   R.sup.5                                                   
                   n Properties                                           
                           TMS as internal reference, δ value       
__________________________________________________________________________
                           (ppm)                                          
36 Me                                                                     
       ##STR35##                                                          
                Me 5 colorless oil                                        
                           1.09 (dq, J=4.0, 12.0Hz, 2H), 1.17-1.34 (m,    
                           4H), 1.42-1.55 (m, 4H), 1.67-1.82 (m, 5H),     
                           1.90 (bd, J=12Hz, 2H), 2.10 (s, 3H), 2.18 (t,  
                           J=8.0Hz, 2H), 2.20 (s, 3H), 2.54 (t, J=8.0Hz,  
                           2H), 3.67 (s, 3H), 3.68 (s, 3H), 3.70 (d,      
                           J=4.0Hz, 2H), 7.22 (t, J=7.6Hz, 1H), 7.46 (d,  
                           J=7.6Hz, 1H), 7.58 (s, 1H), 8.43 (bs, 2H)      
37 Me Me        MeO                                                       
                   4 colorless                                            
                           1.46-1.60 (m, 4H), 2.15 (s, 3H), 2.20 (s, 3H), 
                           2.33 (t, J=8.0Hz, 2H), 2.54                    
                     oil   (t, J=8.0Hz, 2H), 3.53 (s, 3H), 3.69 (s, 3H),  
                           3.75 (s, 3H), 7.19 (d, J=7.5Hz,                
                           1H), 7.44 (d, J=7.5Hz, 1H), 7.63 (s, 1H), 8.42 
                           (bs, 2H)                                       
38 EtO                                                                    
      Me        Me 5 colorless                                            
                           1.23 (m, 2H), 1.39 (t, J=7.0Hz, 3H), 1.46 (m,  
                           2H), 1.52 (m, 2H), 2.08 (s, 3H),               
                     oil   2.17 (s, 3H), 2.20 (t, J=8.0Hz, 2H), 2.53 (t,  
                           J=8.0Hz, 2H), 3.56 (s, 3H), 3.78               
                           (s, 3H), 4.03 (t, J=7.0Hz, 2H), 7.21 (bs, 1H), 
                           7.46 (d, J=8.0Hz, 1H), 7.58 (s,                
                           1H), 8.43 (bs, 2H)                             
__________________________________________________________________________

                                  TABLE 13                                
__________________________________________________________________________
 ##STR36##                                                                
Ex.                     .sup.1 H-NMR spectrum                             
No.                                                                       
   R.sup.3                                                                
          R.sup.4                                                         
             R.sup.5                                                      
                n Properties                                              
                        TMS as internal reference, δ value          
__________________________________________________________________________
                        (ppm)                                             
39                                                                        
    ##STR37##                                                             
          Me Me 5 colorless oil                                           
                        1.20 (tt, J=7.5, 7.5Hz, 2H), 1.40-1.55 (m, 4H),   
                        1.74 (tt, J=7.5, 7.5Hz, 2H), 2.11 (s, 3H), 2.18   
                        (t, J=7.5Hz, 3H), 2.24 (s, 3H), 2.51 (t, J=8.0Hz, 
                        2H), 2.66 (t, J=7.5Hz, 2H), 3.34 (s, 3H), 3.41    
                        (t, J=8.0Hz, 2H), 3.57 (s, 3H), 3.64 (s, 3H),     
                        7.22 (dd, J=4.8, 8.0Hz, 1H), 7.47 (d, J=8.0Hz,    
                        1H), 7.62 (s, 1H), 8.44 (bs, 2H)                  
40 MeS    Me Me 5 pale-yellow                                             
                        1.21 (tt, J=7.5, 7.5Hz, 2H), 1.42-1.65 (m, 4H),   
                        2.13 (s, 3H), 2.19 (t, J=7.5Hz, 2H),              
                  oil   2.39 (s, 3H), 2.43 (s, 3H), 2.53 (t, J=7.5Hz,     
                        2H), 3.58 (s, 3H), 3.79 (s, 3H), 7.22             
                        (dd, J=4.5, 7.5Hz, 1H), 7.47 (d, J=7.5Hz, 1H),    
                        7.58 (s, 1H), 8.40-8.51 (m, 2H)                   
41 MOMO   Me Me 5 pale-yellow                                             
                        1.24 (tt, J=7.5, 7.5Hz, 2H), 1.45 (tt, J=7.5,     
                        7.5Hz, 2H), 1.52 (tt, J=7.5, 7.5Hz, 2H),          
                  oil   2.08 (s, 3H), 2.20 (t, J=7.5Hz, 2H), 2.21 (s,     
                        3H), 2.53 (t, J=7.5Hz, 2H), 3.56 (s, 3H),         
                        3.60 (s, 3H), 3.72 (s, 3H), 5.11 (s, 2H), 7.11    
                        (dd, J=4.5, 7.5Hz, 1H), 7.47 (d, J=               
                        7.5Hz, 1H), 7.57 (s, 1H), 8.40-8.48 (bs,          
__________________________________________________________________________
                        2H)
EXAMPLE 42 (E)-3-(4-Hydroxy-2,5-dimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid ##STR38##
1.85 g of the compound prepared in the Example 41 was dissolved in 15 ml of acetone, followed by the addition of 2.5 ml of concentrated hydrochloric acid. The obtained mixture was stirred at room temperature for 10 hours, neutralized with a saturated aqueous solution of sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and filtered. The filtrate was distilled to remove the solvent. 7.59 g of the title compound was obtained as a white glassy substance.
1 H-NMR (CDCl3) δ (ppm); 1.21 (tt, J=7.5, 7.5 Hz, 2H), 1.49 (tt, J=7.5, 7.5 Hz, 2H), 2.12 (s, 3H), 2.17 (s, 3H), 2.02 (t, J=7.5 Hz, 2H), 2.50 (t, J=7.5 Hz, 2H), 3.56 (s, 3H), 3.74 (s, 3H), 7.18-7.28 (m, 1H), 7.24 (d, J=5.5 Hz, 1H), 7.39 (s, 1H), 8.35-8.50 (m, 2H).
EXAMPLE 43 (E)-3-(2-Hydroxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid hydrochloride ##STR39##
1.26 g of the (E)-3-(4-hydroxy-2,5-dimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid prepared in the Example 42 was dissolved in an acetonitrile (60 ml)/water (30 ml) mixture. The obtained solution was cooled to ice temperature, followed by the gradual dropwise addition of 20 ml of an aqueous solution of 3.63 g of cerium (IV) ammonium nitrate. A 5% aqueous solution of sodium hydrogencarbonate was added to the resulting solution to adjust the pH to 6. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and filtered. 1.6 ml of 6N hydrochloric acid and 100 ml of ethanol were added to the filtrate and the solvent was distilled away in a vacuum. The residue was recrystallized from ethanol to give 0.80 g of the title compound as a yellow crystal.
1 H-NMR (DMSO-d6) δ (ppm); 1.05-1.18 (m, 2H), 1.20-1.38 (m, 2H), 1.40-1.54 (m, 2H), 1.73 (s, 3H), 1.80 (s, 3H), 2.00 (bt, J=7.0 Hz, 2H), 2.66 (t, J=7.0 Hz, 2H), 7.04 (bs, 1H), 7.91 (dd, J=5.0, 8.0 Hz, 1H), 8.35 (bd, J=8.0 Hz, 1H), 8.65-8.80 (m, 1H), 8.75 (s, 1H).
MS; 370 (MH+).
EXAMPLES 44 TO 62
The compounds listed in the following Tables 14 to 20 were each prepared in a similar manner to that of the Example 3:
                                  TABLE 14                                
__________________________________________________________________________
 ##STR40##                                                                
Ex.                     .sup.1 H-NMR spectrum                             
No.                                                                       
   R.sup.3                                                                
        R.sup.4                                                           
           R.sup.5                                                        
              n Properties                                                
                        TMS as internal reference, δ value          
__________________________________________________________________________
                        (ppm)                                             
44 n-HepO                                                                 
        Me Me 5 yellow  0.76 (t, J=7.0Hz, 3H), 1.20-1.40 (m, 8H),         
                        1.40-1.55 (m, 4H), 1.60 (tt, J=7.0, 7.0Hz,        
                oil     2H), 1.74 (tt, J=7.0, 7.0Hz, 2H), 1.95 (s, 3H),   
                        1.99 (s, 3H), 2.13 (t, J=7.0Hz, 2H),              
                        2.60 (t, J=7.0Hz, 2H), 4.20 (t, J=7.0Hz, 2H),     
                        7.23 (s, 1H), 7.25 (dd, J=5.0, 8.0Hz,             
                        1H), 7.53 (bd, J=8.0Hz, 1H), 8.43 (d, J=5.0Hz,    
                        1H), 8.49 (bs, 1H)                                
45 MeO  Me Me 5 yellow crystal                                            
                        1.26 (tt, J=7.0, 7.0Hz, 2H), 1.50 (tt, J=7.0,     
                        7.0Hz, 2H), 1.61 (tt, J=7.0, 7.0Hz, 2H),          
                m.p.:   1.95 (s, 3H), 1.96 (s, 3H), 2.12 (t, J=7.0Hz,     
                        2H), 2.60 (t, J=7.0Hz, 2H), 4.01 (s,              
                134-135° C.                                        
                        3H), 7.26 (s, 1H), 7.27 (dd, J=5.0, 8.5Hz, 1H),   
                        7.55 (bd, J=8.5Hz, 1H), 8.44 (bd,                 
                        J=5.0Hz, 1H), 8.50 (bs, 1H)                       
46 Me   MeO                                                               
           Me 5 yellow crystal                                            
                        1.27 (tt, J=7.6, 7.6Hz, 2H), 1.51 (tt, J=7.6,     
                        7.6Hz, 2H), 1.61 (tt, J=7.6, 7.6Hz, 2H),          
                m.p.:   1.97 (s, 3H), 1.98 (s, 3H), 2.13 (t, J=7.2Hz,     
                        2H), 2.61 (t, J=8.0Hz, 2H), 3.98 (s, 3H),         
                128-130° C.                                        
                        7.23 (s, 1H), 7.28 (dd, J=2.4, 7.2Hz, 1H), 8.45   
                        (d, J=4.8Hz, 1H), 8.90 (s, 1H)                    
__________________________________________________________________________

                                  TABLE 15                                
__________________________________________________________________________
 ##STR41##                                                                
Ex.                     .sup.1 H-NMR spectrum                             
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
           R.sup.5                                                        
              n Properties                                                
                        TMS as internal reference, δ value          
__________________________________________________________________________
                        (ppm)                                             
47 Me n-BuO                                                               
           Me 5 yellow crystal                                            
                        0.95 (t, J=7.4Hz, 3H), 1.26 (tt, J=7.6, 7.6Hz,    
                        2H), 1.40-1.52 (m, 4H), 1.60 (tt, J=              
                m.p.:   7.6, 7.6Hz, 2H), 1.70 (tt, J=7.6, 7.6Hz, 2H),     
                        1.99 (s, 3H), 2.00 (s, 3H), 2.13 (t, J=           
                97-100° C.                                         
                        8.0Hz, 2H), 2.60 (t, J=8.0Hz, 2H), 4.20 (t,       
                        J=8.0Hz, 2H), 7.24 (s, 1H), 7.28 (dd,             
                        J=2.4, 7.6Hz, 1H), 7.55 (d, J=6.4Hz, 1H), 8.45    
                        (d, J=4.0Hz, 1H), 8.49 (s, 1H)                    
48 Me n-BuO                                                               
           Me 3 yellow crystal                                            
                        0.95 (t, J=6.8Hz, 3H), 1.45 (q, J=7.2Hz, 2H),     
                        1.70 (tt, J=4.8, 4.8Hz, 2H), 1.90                 
                m.p.:   (bs, 2H), 1.95 (s, 3H), 1.99 (s, 3H), 2.13-2.27   
                        (m, 2H), 2.53-2.66 (m, 2H), 4.12 (t,              
                92-95° C.                                          
                        J=7.6Hz, 2H), 7.25 (bs, 2H), 7.53 (d, J=6.0Hz,    
                        1H), 8.43 (bs, 1H), 8.61 (bs, 1H)                 
49 Me n-HepO                                                              
           Me 5 yellow  0.87 (t, J=8.0Hz, 3H), 1.22-1.36 (m, 8H), 1.39    
                        (tt, J=7.6, 7.6Hz, 2H), 1.49 (tt, J=              
                oil     7.6, 7.6Hz, 2H), 1.60 (tt, J=7.6, 7.6Hz, 2H),     
                        1.70 (q, J=8.0Hz, 2H), 1.97 (s, 3H), 1.99         
                        (s, 3H), 2.14 (t, J=7.6Hz, 2H), 2.60 (t, J=7.6Hz, 
                        2H), 4.08 (t, J=8.0Hz, 2H), 7.24                  
                        (d, J=4.8Hz, 1H), 7.28 (s, 1H), 7.54 (d, J=7.6Hz, 
                        1H), 8.44 (d, J=4.8Hz, 1H), 8.48 (s,              
__________________________________________________________________________
                        1H)                                               

                                  TABLE 16                                
__________________________________________________________________________
 ##STR42##                                                                
Ex.                   .sup.1 H-NMR spectrum                               
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                      TMS as internal reference, δ value            
__________________________________________________________________________
                      (ppm)                                               
50 Me EtO                                                                 
         Me 5 yellow crystal                                              
                      1.26 (tt, J=7.6, 7.6Hz, 2H), 1.34 (t, J=6.8Hz, 3H), 
                      1.50 (tt, J=7.6, 7.6Hz, 2H), 1.59 (tt,              
              m.p.:   J=7.6, 7.6Hz, 2H), 1.97 (s, 3H), 1.98 (s, 3H), 2.13 
                      (t, J=7.2Hz, 2H), 2.59 (t, J=8.0Hz,                 
              105-108° C.                                          
                      2H), 4.26 (q, J=7.2Hz, 2H), 7.24 (s, 1H), 7.29 (dd, 
                      J=2.8, 7.6Hz, 1H), 7.561 (d,                        
                      J=7.6Hz, 1H), 8.46 (d, J=4.8Hz, 1H), 8.48 (s, 1H)   
51 MeO                                                                    
      Me Me 3 yellow crystal                                              
                      1.90 (tt, J=8.0, 8.0Hz, 2H), 1.95 (s, 3H), 1.97 (s, 
                      3H), 2.17 (t, J=8.0Hz, 2H), 2.63 (t,                
              m.p.:   J=8.0Hz, 2H), 4.04 (s, 3H), 7.26 (s, 1H), 7.28 (dd, 
                      J=4.5, 7.5Hz, 1H), 7.56 (bd, J=                     
              140-142° C.                                          
                      7.5Hz, 1H), 8.47 (bd, J=4.5Hz, 1H), 8.64 (bs, 1H)   
52 Me Me MeO                                                              
            5 yellow crystal                                              
                      1.28 (tt, J=7.5, 7.5Hz, 2H), 1.51 (tt, J=7.5,       
                      7.5Hz, 2H), 1.60 (tt, J=7.5, 7.5Hz, 2H),            
              m.p.:   2.03 (s, 3H), 2.04 (s, 3H), 2.18 (t, J=7.5Hz, 2H),  
                      2.59 (t, J=7.5Hz, 2H), 3.96 (s, 3H),                
              148-149° C.                                          
                      7.27 (dd, J=5.0, 8.0Hz, 1H), 7.30 (s, 1H), 7.55     
                      (bd, J=8.0Hz, 1H), 8.45 (dd, J=1.5,                 
                      5.0Hz, 1H), 8.48 (d, J=1.5Hz, 1H)                   
__________________________________________________________________________

                                  TABLE 17                                
__________________________________________________________________________
 ##STR43##                                                                
Ex.                   .sup.1 H-NMR spectrum                               
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                      TMS as internal reference, δ value            
__________________________________________________________________________
                      (ppm)                                               
53 MeO                                                                    
      Me Me 4 yellow crystal                                              
                      1.42-1.63 (m, 4H), 1.95 (s, 6H), 2.17 (t, J=7.0Hz,  
                      2H), 2.62 (t, J=7.0Hz, 2H), 4.03 (s,                
              m.p.:   3H), 7.25 (s, 1H), 7.31 (dd, J=5.0, 8.0Hz, 1H),     
                      7.60 (d, J=8.0Hz, 1H), 8.46 (bd, J=                 
              124-125° C.                                          
                      5.0Hz, 1H), 8.48 (bs, 1H)                           
54 MeO                                                                    
      Me Me 6 yellow crystal                                              
                      1.15-1.34 (m, 4H), 1.44 (tt, J=7.5, 7.5Hz, 2H),     
                      1.58 (tt, J=7.5, 7.5Hz, 2H), 1.95 (s, 6H),          
              m.p.:   2.12 (t, J=7.5Hz, 2H), 2.60 (t, J=7.5Hz, 2H), 4.03  
                      (s, 3H), 7.25 (s, 1H), 7.32 (dd, J=5.5,             
              119-121° C.                                          
                      8.0Hz, 1H), 7.60 (d, J=8.0Hz, 1H), 8.47 (dd, J=1.0, 
                      5.5Hz, 1H), 8.50 (d, J=1.0Hz, 1H)                   
55 Me MeO                                                                 
         Me 6 yellow crystal                                              
                      1.19-1.33 (m, 4H), 1.45 (tt, J=7.2, 7.2Hz, 2H),     
                      1.58 (tt, J=6.8, 6.8Hz, 2H), 1.97 (s, 3H),          
              m.p.:   1.98 (s, 3H), 2.13 (t, J=7.6Hz, 2H), 2.60 (t,       
                      J=8.0Hz, 2H), 4.99 (s, 3H), 7.24 (d, J=             
              108-110° C.                                          
                      1.2Hz, 1H), 7.29 (dd, J=2.4, 7.2Hz, 1H), 7.57 (d,   
                      J=8.0Hz, 1H), 8.46 (d, J=4.8Hz,                     
                      1H), 8.49 (s, 1H)                                   
__________________________________________________________________________

                                  TABLE 18                                
__________________________________________________________________________
 ##STR44##                                                                
Ex.                   .sup.1 H-NMR spectrum                               
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
         R.sup.5                                                          
            n Properties                                                  
                      TMS as internal reference, δ value            
__________________________________________________________________________
                      (ppm)                                               
56 Me Me MeO                                                              
            6 yellow crystal                                              
                      1.20-1.31 (m, 4H), 1.43 (tt, J=7.5, 7.5Hz, 2H),     
                      1.56 (tt, J=7.5, 7.5Hz, 2H), 2.01 (s,               
              m.p.:   3H), 2.03 (s, 3H), 2.15 (t, J=7.5Hz, 2H), 2.55 (t,  
                      J=7.5Hz, 2H), 3.94 (s, 3H), 7.25 (t, J=             
              64-66° C.                                            
                      8.0Hz, 1H), 7.27 (s, 1H), 7.53 (d, J=8.0Hz, 1H),    
                      8.46 (bs, 2H)                                       
57 H  Me MeO                                                              
            5 yellow crystal                                              
                      1.14 (tt, J=8.0, 8.0Hz, 2H), 1.34 (tt, J=8.0,       
                      8.0Hz, 2H), 1.45 (tt, J=8.0, 8.0Hz, 2H), 1.93 (s,   
                      3H),                                                
              m.p.:   2.03 (t, J=8.0Hz, 2H), 2.48 (t, J=8.0Hz, 2H), 3.91  
                      (s, 3H), 6.67 (s, 1H), 6.99 (s, 1H),                
              110-112° C.                                          
                      7.24 (dd, J=4.0, 7.0Hz, 1H), 7.53 (dt, J=1.0,       
                      4.0Hz, 1H), 8.34 (bs, 2H)                           
58 Me Me Me 5 yellow crystal                                              
                      1.18-1.31 (m, 2H), 1.40 (m, 4H), 1.97 (s, 3H), 2.03 
                      (s, 3H), 2.05 (s, 3H), 2.12 (t, J=                  
              m.p.:   7.2Hz, 2H), 2.60 (t, J=8.0Hz, 2H), 7.22-7.35 (m,    
                      1H), 7.27 (s, 1H), 7.58 (d, J=7.6Hz,                
              152-154° C.                                          
                      1H), 8.38-8.60 (m, 2H)                              
__________________________________________________________________________

                                  TABLE 19                                
__________________________________________________________________________
 ##STR45##                                                                
Ex.                          .sup.1 H-NMR spectrum                        
No.                                                                       
   R.sup.3                                                                
      R.sup.4   R.sup.5                                                   
                   n Properties                                           
                             TMS as internal reference, δ value     
                             (ppm)                                        
__________________________________________________________________________
59 Me                                                                     
       ##STR46##                                                          
                Me 5 yellow oil                                           
                             1.02 (dq, J=4.0, 12.0Hz, 2H), 1.20-1.30 (m,  
                             4H), 1.49 (tt, J=8.0, 8.0Hz, 2H), 1.59 (tt,  
                             J=8.0, 8.0Hz, 2H), 1.65-1.85 (m, 7H), 1.95   
                             (s, 3H), 1.98 (s, 3H), 2.12 (t, J=8.0Hz,     
                             2H), 2.59 (t, J=8.0Hz, 2H), 3.99 (d, J=      
                             8.0Hz, 2H), 7.23 (s, 1H), 7.27 (d, J=7.2Hz,  
                             1H), 7.53 (d, J=7.2Hz, 1H), 8.45 (bs, 1H),   
                             8.49 (bs, 1H)                                
60 Me Me        MeO                                                       
                   4 yellow crystal                                       
                             1.36 (tt, J=8.0, 8.0Hz, 2H), 1.46 (tt,       
                             J=8.0, 8.0Hz, 2H), 1.92 (s, 3H),             
                     m.p.:   1.96 (s, 3H), 2.09 (t, J=8.0Hz, 2H), 2.50    
                             (t, J=8.0Hz, 2H), 3.86 (s, 3H),              
                     164-166° C.                                   
                             7.01 (s, 1H), 7.25 (dd, J=4.8, 7.6Hz, 1H),   
                             7.52 (d, J=7.6Hz, 1H), 8.33                  
                             (s, 1H), 8.35 (d, J=4.8Hz, 1H)               
61 EtO                                                                    
      Me        Me 5 yellow crystal                                       
                             1.26 (m, 2H), 1.38 (t, J=7.0Hz, 3H), 1.50    
                             (m, 2H), 1.60 (m, 2H), 1.95 (s,              
                     m.p.:   3H), 1.96 (s, 3H), 2.12 (t, J=8.0Hz, 2H),    
                             2.60 (t, J=8.0Hz, 2H), 4.28 (q,              
                     116-118° C.                                   
                             J=7.0Hz, 2H), 7.25-7.29 (m, 2H), 7.55 (dt,   
                             J=8.0, 1.0Hz, 1H), 8.45                      
                             (dd, J=5.0, 1.0Hz, 1H), 8.50 (d, J=1.0Hz,    
__________________________________________________________________________
                             1H)                                          

                                  TABLE 20                                
__________________________________________________________________________
 ##STR47##                                                                
Ex.                     .sup.1 H-NMR spectrum                             
No.                                                                       
   R.sup.3                                                                
      R.sup.4                                                             
             R.sup.5                                                      
                n Properties                                              
                        TMS as internal reference, δ value          
__________________________________________________________________________
                        (ppm)                                             
62 Me                                                                     
       ##STR48##                                                          
             Me 5 yellow oil                                              
                        1.15 (tt, J=7.5, 7.5Hz, 2H), 1.31 (tt, J=7.5,     
                        7.5Hz, 2H), 1.43-1.58 (m, 4H), 1.83 (s, 3H), 1.96 
                        (s, 3H), 1.99 (t, J=7.5Hz, 2H), 2.43 (t, J=8.0Hz, 
                        2H), 2.67 (t, J= 7.5Hz, 2H), 3.16 (s, 3H), 3.24   
                        (t, J=8.0Hz, 2H), 7.05 (s, 1H), 7.93 (t, J=7.5Hz, 
                        1H), 8.35 (d, J=7.5Hz, 1H), 8.72 (bs,             
__________________________________________________________________________
                        2H)
EXAMPLE 63 Ethyl 3-(2-methoxy-3,5-dimethyl-1,4-benzoquinon-6-yl)-2-[5-(3-pyridyl)pentyl]propenoate hydrochloride ##STR49##
1 g of the compound prepared in the Example 46 was dissolved in 10 ml of ethanol, followed by the addition of 0.7 ml of concentrated sulfuric acid. The obtained mixture was heated under reflux for 12 hours, cooled, neutralized and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated in a vacuum. The residue was purified by silica gel column chromatography [ethyl acetate (0→30%)/hexane]. The residue was dissolved in a small amount of ethanol, followed by the addition of 0.25 ml of concentrated hydrochloric acid. The obtained mixture was concentrated in a vacuum to give the title compound as a yellow oil.
1 H-NMR (400 MHz, DMSO-d6) δ (ppm); 1.17 (tt, J=8.0, 8.0 Hz, 2H), 1.27 (t, J=6.4 Hz, 3H), 1.36 (tt, J=8.0, 8.0 Hz, 2H), 1.55 (tt, J=8.0, 8.0 Hz, 2H), 1.85 (s, 3H), 1.88 (s, 3H), 2.07 (t, J=8.0 Hz, 2H), 2.73 (t, J=8.0 Hz, 2H), 3.88 (s, 3H), 4.20 (q, J=6.4 Hz, 2H), 7.06 (s, 1H), 8.00 (dd, J=1.6, 8.0 Hz, 1H), 8.45 (d, J=8.0 Hz, 1H), 8.78 (d, J=5.2 Hz, 1H), 8.81 (s, 1H).
EXAMPLE 64 3-(2-Methoxy-3,5-dimethyl-1,4-benzoquinon-6-yl)-2-[5-(3-pyridyl)pentyl]-1-oxo-1 -morpholinyl-2-propene ##STR50##
1.4 g of the compound prepared in the Example 46 was dissolved in 200 ml of dichloromethane. The obtained solution was washed with 100 ml of a 10% aqueous solution of sodium hydrosulfite twice. The dichloromethane layer was dried over anhydrous magnesium sulfate and concentrated in a vacuum. 20 ml of N,N-dimethylformamide and 1 g of sodium hydrosulfite were added to the residue. The obtained mixture was cooled to 0° C., followed by the dropwise addition of 1.1 g of diphenylphosphorylazide, 0.32 g of morpholine and 0.38 g of triethylamine in this order. The obtained mixture was stirred at room temperature day and night, followed by the addition of water. The obtained mixture was extracted with ethyl acetate. The organic layer was stirred while bubbling air thereinto for 2 hours, washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated in a vacuum. The residue was purified by silica gel column chromatography (ethyl acetate) to give 0.71 g of the title compound as an orange oil.
1 H-NMR (400 MHz, CDCl3) δ (ppm); 1.27 (tt, J=8.0, 8.0 Hz, 2H), 1.36 (tt, J=8.0, 8.0 Hz, 2H), 1.55 (tt, J=8.0, 8.0 Hz, 2H), 1.98 (s, 6H), 2.10 (t, J=8.0 Hz, 2H), 2.55 (t, J=8.0 Hz, 2H), 3.65-3.80 (m, 8H), 3.96 (s, 3H), 5.97 (d, J=1.2 Hz, 1H), 7.18 (dd, J=3.6, 8.0 Hz, 1H), 7.44 (dt, J=1.2, 8.0 Hz, 1H), 8.39 (d, J=1.5 Hz, 1H), 8.42 (dd, J=1.5, 3.6 Hz, 1H).
TOXICITY TEST (1) Repetitive Oral Administration Test for 4 Weeks on Rats Method
30 and 100 mg/kg of the compound obtained in the Example 3 was orally administered to female Slc:SD rats aged 7 weeks (each group consisting of 5 animals) for 4 weeks. This compound was suspended in a 0.5 wt. % aqueous solution of methylcellulose and administered once a day.
During the administration period, the general conditions of the animals were observed and the body weight and feed intake were measured. After the completion of the final administration, hematological examination, hemo-biochemical examination, urinalysis and autopsy were effected and organs were weighed. Further, livers and kidneys were patho-histologically examined under an optical microscope.
Results
No change was observed at each of the doses of 30 and 100 mg/kg.
TOXICITY TEST (2) Repetitive Oral Administration Test for 4 Weeks on Dogs Method
30 and 100 mg/kg of the compound obtained in the Example 3 was orally administered to female beagles aged 8 months (each group consisting of 2 animals) for 4 weeks. This compound was triturated with lactose and administered once a day.
During the administration period, the general conditions of the animals were observed and the body weight and feed intake were measured. After the completion of the first, seventh and final administrations, hemo-biochemical examination was effected. After the completion of the seventh and final administrations, further, hematological examination and urinalysis were effected. Furthermore, autopsy was effected and organs were weighed after the final administration. Livers, kidneys and adrenal bodies were patho-histologically examined under an optical microscope.
Results
No change was observed at each of the doses of 30 and 100 mg/kg.
Thus the toxicologically non-influential dose of the compound obtained in the Example 3 was judged to be 100 mg/kg.

Claims (28)

What we claim is:
1. A quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR51## wherein A stands for a group represented by the formula: ##STR52## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group, or a group represented by the formula: ##STR53## ##STR54## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group; X and Y are the same or different from each other and each stand for a hydroxyl group or a protected hydroxyl group; R1 stands for a heteroarylalkyl group selected from the group consisting of a pyridylalkyl group and an imidazolylalkyl group; and B stands for a carboxyl group or a protected carboxyl group.
2. Leukotrienes production inhibitor comprising a quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 as an active ingredient.
3. Thromboxanes production inhibitor comprising a quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 as an active ingredient.
4. A therapeutic agent for treating diseases for which leukotrienes production inhibitor is efficacious, which comprises a quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 as an active ingredient.
5. A therapeutic agent for treating diseases for which thromboxanes inhibitor is efficacious, which comprises a quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 as an active ingredient.
6. A pharmacological composition which comprises a therapeutically effective amount of the quinone derivative or a pharmacologically acceptable salt thereof as set forth in claim 1 and a pharmacologically acceptable vehicle.
7. A method of using a quinone derivative or a pharmacologically acceptable salt thereof as set forth in claim 1 comprising the step of making a medicament containing said quinone derivative as an active ingredient for treating a disease in which the production of leukotriene is elevated.
8. A method of using a quinone derivative or a pharmacologically acceptable salt thereof as set forth in claim 1 comprising the step of making a medicament containing said quinone derivative as an active ingredient for treating a disease in which the production of thromboxane A2 is elevated.
9. A method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 to a patient suffering from a disease in which the production of leukotriene is elevated.
10. A method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 to a patient suffering from a disease in which the production of thromboxane A2 is elevated.
11. A method for treating a disease which comprises administering a pharmaceutically effective amount of the quinone derivative or pharmacologically acceptable salt thereof as set forth in claim 1 to a patient suffering from a disease selected from the group consisting of asthma, myocardial infarction, angina pectoris, cerebral embolism, cerebral thrombosis, renal insufficiency, nephrosis and nephritis.
12. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein R3 is a lower alkoxy group.
13. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein R4 is a lower alkyl group.
14. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein R5 is a lower alkyl group.
15. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein X is a hydroxy group or a alkoxy group.
16. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein Y is a hydroxy group or a alkoxy group.
17. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein B is a carboxyl group.
18. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein R3 is a methoxy group or a methyl group.
19. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein R4 is a methyl group or a methoxy group.
20. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein R5 is a methyl group or a methoxy group.
21. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein X is a hydroxy group or a methoxy group.
22. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 1, wherein Y is a hydroxy group or a methoxy group.
23. A quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR55## wherein A stands for a group represented by the formula: ##STR56## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group, or a group represented by the formula: ##STR57## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group; X and Y are the same or different from each other and each stand for a hydroxyl group or a protected hydroxyl group R1 stands for a 5 or 6 membered nitrogen-containing heteroarylalkyl group selected from the group consisting of a pyridylalkyl group and an imidazolylalkyl group; and B stands for a carboxyl group or a protected carboxyl group.
24. A quinone derivative or pharmacologically acceptable salt thereof as claimed in claim 23, wherein R1 is an imidazolylalkyl group.
25. A quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR58## wherein A stands for a group represented by the formula: ##STR59## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group, or a group represented by the formula: ##STR60## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, an alkoxyalkoxy group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group; X and Y are the same or different from each other and each stand for a hydroxyl group or a protected hydroxyl group; R1 is a pyridylhexyl group or a pyridylpentyl group; and B stands for a carboxyl group or a protected carboxyl group.
26. A quinone derivative or pharmacologically acceptable salt thereof wherein the quinone derivative is selected from the group consisting of the below listed quinone derivatives:
(E)-3-(2-Methoxy-3,5-dimethyl-1,4-benzoquinon-6-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2-Methoxy-5,6-dimethyl-1,4-benzoquinon-3-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2-Methoxy-5,6-dimethyl-1,4-benzoquinon-3-yl)-2-[6-(3-pyridyl)hexyl]-2-propenoic acid
(E)-3-(2,4,5-Trimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2,5-Dihydroxy-4-methoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid
(E)-3-(2,3,5-Trimethoxy-4,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid.
27. A quinone derivative or pharmacologically acceptable salt thereof wherein the quinone derivative is (E)-3-(2-methoxy-3,6-dimethyl-1,4-benzoquinon-5-yl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid.
28. A quinone derivative represented by the following general formula (I) or a pharmacologically acceptable salt thereof: ##STR61## wherein A stands for a group represented by the formula: ##STR62## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneous each a lower alkoxy group, or a group represented by the formula: ##STR63## wherein R3, R4 and R5 are the same or different from each other and each stand for a hydrogen atom, a hydroxyl group, a lower alkyl group, a lower alkoxy group, an alkoxyalkyl group, a cycloalkylalkoxy group, a thiol group or a thioalkyl group, with the proviso that R3 and R4 are not simultaneously each a lower alkoxy group; X and Y are the same or different from each other and each stands for a hydroxyl group or a protected hydroxyl group; R1 is a pyridylalkyl group; and B stands for a carboxyl group or a protected carboxyl group.
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US9359275B2 (en) 2012-02-23 2016-06-07 Children's Medical Center Corporation Natural product antibiotics and analogs thereof

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US20050215728A1 (en) * 2001-03-13 2005-09-29 Dais-Analytic Corporation Crosslinked polymer electrolyte membranes for heat, ion and moisture exchange devices
US7179860B2 (en) * 2001-03-13 2007-02-20 Liwei Cao Crosslinked polymer electrolyte membranes for heat, ion and moisture exchange devices
US9359275B2 (en) 2012-02-23 2016-06-07 Children's Medical Center Corporation Natural product antibiotics and analogs thereof

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